TW202222946A - Structure for manufacturing cast article - Google Patents
Structure for manufacturing cast article Download PDFInfo
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- TW202222946A TW202222946A TW110138503A TW110138503A TW202222946A TW 202222946 A TW202222946 A TW 202222946A TW 110138503 A TW110138503 A TW 110138503A TW 110138503 A TW110138503 A TW 110138503A TW 202222946 A TW202222946 A TW 202222946A
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- Taiwan
- Prior art keywords
- mass
- less
- casting
- inorganic particles
- fibers
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 98
- 239000000835 fiber Substances 0.000 claims abstract description 201
- 239000010954 inorganic particle Substances 0.000 claims abstract description 108
- 238000005452 bending Methods 0.000 claims abstract description 47
- 230000009467 reduction Effects 0.000 claims abstract description 28
- 239000012299 nitrogen atmosphere Substances 0.000 claims abstract description 8
- 238000005266 casting Methods 0.000 claims description 156
- 239000002245 particle Substances 0.000 claims description 49
- 239000012784 inorganic fiber Substances 0.000 claims description 40
- 229920005989 resin Polymers 0.000 claims description 23
- 239000011347 resin Substances 0.000 claims description 23
- 238000002844 melting Methods 0.000 claims description 20
- 230000008018 melting Effects 0.000 claims description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 14
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 8
- 229920001225 polyester resin Polymers 0.000 claims description 7
- 239000004645 polyester resin Substances 0.000 claims description 7
- 239000004760 aramid Substances 0.000 claims description 6
- 229920003235 aromatic polyamide Polymers 0.000 claims description 6
- 239000000377 silicon dioxide Substances 0.000 claims description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 4
- 239000012798 spherical particle Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 description 43
- 239000002184 metal Substances 0.000 description 42
- 239000002734 clay mineral Substances 0.000 description 38
- 239000007789 gas Substances 0.000 description 32
- 239000002243 precursor Substances 0.000 description 28
- 239000000463 material Substances 0.000 description 27
- 230000007547 defect Effects 0.000 description 25
- 230000035515 penetration Effects 0.000 description 22
- 238000000034 method Methods 0.000 description 21
- 230000014759 maintenance of location Effects 0.000 description 17
- 238000011156 evaluation Methods 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 229920000049 Carbon (fiber) Polymers 0.000 description 15
- 239000004917 carbon fiber Substances 0.000 description 15
- 238000010438 heat treatment Methods 0.000 description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 14
- 229920001131 Pulp (paper) Polymers 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 13
- 239000002612 dispersion medium Substances 0.000 description 13
- 238000002156 mixing Methods 0.000 description 10
- 229920001187 thermosetting polymer Polymers 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 9
- -1 polyethylene Polymers 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 8
- 239000005011 phenolic resin Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 239000010439 graphite Substances 0.000 description 7
- 229910002804 graphite Inorganic materials 0.000 description 7
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 6
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical group O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000000440 bentonite Substances 0.000 description 5
- 229910000278 bentonite Inorganic materials 0.000 description 5
- 230000002950 deficient Effects 0.000 description 5
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 5
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 238000004898 kneading Methods 0.000 description 5
- 229910052901 montmorillonite Inorganic materials 0.000 description 5
- 229910052863 mullite Inorganic materials 0.000 description 5
- 229920002239 polyacrylonitrile Polymers 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 238000010298 pulverizing process Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 4
- 238000005336 cracking Methods 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical group O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
- 239000005332 obsidian Substances 0.000 description 4
- 239000010893 paper waste Substances 0.000 description 4
- 238000013001 point bending Methods 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 229920002994 synthetic fiber Polymers 0.000 description 4
- 239000012209 synthetic fiber Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005304 joining Methods 0.000 description 3
- 229910052622 kaolinite Inorganic materials 0.000 description 3
- 229910052618 mica group Inorganic materials 0.000 description 3
- 239000002557 mineral fiber Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 229920003987 resole Polymers 0.000 description 3
- 238000000371 solid-state nuclear magnetic resonance spectroscopy Methods 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 2
- 241000218631 Coniferophyta Species 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000011304 carbon pitch Substances 0.000 description 2
- 238000003763 carbonization Methods 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000002149 energy-dispersive X-ray emission spectroscopy Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 238000013507 mapping Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229920000747 poly(lactic acid) Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920005678 polyethylene based resin Polymers 0.000 description 2
- 239000004626 polylactic acid Substances 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 238000012805 post-processing Methods 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 241000283707 Capra Species 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Chemical group 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920000331 Polyhydroxybutyrate Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- UJOHNXQDVUADCG-UHFFFAOYSA-L aluminum;magnesium;carbonate Chemical compound [Mg+2].[Al+3].[O-]C([O-])=O UJOHNXQDVUADCG-UHFFFAOYSA-L 0.000 description 1
- HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 description 1
- 229910021383 artificial graphite Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 210000000085 cashmere Anatomy 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- HDNHWROHHSBKJG-UHFFFAOYSA-N formaldehyde;furan-2-ylmethanol Chemical compound O=C.OCC1=CC=CO1 HDNHWROHHSBKJG-UHFFFAOYSA-N 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 229910052621 halloysite Inorganic materials 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical group NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910000273 nontronite Inorganic materials 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000002006 petroleum coke Substances 0.000 description 1
- 239000005014 poly(hydroxyalkanoate) Substances 0.000 description 1
- 239000005015 poly(hydroxybutyrate) Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920002961 polybutylene succinate Polymers 0.000 description 1
- 239000004631 polybutylene succinate Substances 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000903 polyhydroxyalkanoate Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 229910000275 saponite Inorganic materials 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 238000010112 shell-mould casting Methods 0.000 description 1
- 229910052604 silicate mineral Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- XQQWBPOEMYKKBY-UHFFFAOYSA-H trimagnesium;dicarbonate;dihydroxide Chemical compound [OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[O-]C([O-])=O.[O-]C([O-])=O XQQWBPOEMYKKBY-UHFFFAOYSA-H 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/02—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by additives for special purposes, e.g. indicators, breakdown additives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/02—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by additives for special purposes, e.g. indicators, breakdown additives
- B22C1/04—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by additives for special purposes, e.g. indicators, breakdown additives for protection of the casting, e.g. against decarbonisation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
- B22C1/18—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of inorganic agents
- B22C1/181—Cements, oxides or clays
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C9/00—Moulds or cores; Moulding processes
- B22C9/08—Features with respect to supply of molten metal, e.g. ingates, circular gates, skim gates
- B22C9/082—Sprues, pouring cups
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mold Materials And Core Materials (AREA)
Abstract
Description
本發明係關於一種鑄物製造用結構體。The present invention relates to a structure for manufacturing a cast product.
用於鑄造鑄物之鑄模典型的是使用木模、金屬模或砂模,關於該等鑄模,理想的是,提高成形性或形狀保持性、輕量化及降低廢棄處理成本等。本申請人提出了一種鑄物製造用結構體,其含有無機纖維、層狀黏土礦物及除該層狀黏土礦物以外之無機粒子,並且有機成分之含量為特定量以下(專利文獻1)。 先前技術文獻 專利文獻 A wood mold, a metal mold, or a sand mold is typically used for casting molds, and these molds are desirably improved in formability and shape retention, lightweight, and reduced in disposal cost. The present applicant proposes a structure for producing a cast, which contains inorganic fibers, a layered clay mineral, and inorganic particles other than the layered clay mineral, and has an organic component content of a specific amount or less (Patent Document 1). prior art literature Patent Literature
專利文獻1:US 2020346279 A1Patent Document 1: US 2020346279 A1
本發明係關於一種鑄物製造用結構體。 於一實施方式中,上述結構體含有有機成分。 於一實施方式中,上述結構體中上述有機成分之至少一部分為有機纖維。 於一實施方式中,上述結構體於氮氣氛圍下以1000℃加熱30分鐘後之質量減少率為1質量%以上且未達20質量%。 於一實施方式中,含有無機粒子。 於一實施方式中,無機粒子包含非層狀粒子之第1無機粒子、及作為層狀粒子之第2無機粒子。 於一實施方式中,無機粒子包含熔點為1200℃以上之第1無機粒子、及熔點未達1200℃之第2無機粒子。 於一實施方式中,依據JIS K7017測定之最大彎曲應力為9 MPa以上。 於一實施方式中,依據JIS K7017測定之最大彎曲應力時之彎曲應變為0.6%以上。 The present invention relates to a structure for manufacturing a cast product. In one Embodiment, the said structure contains an organic component. In one embodiment, at least a part of the organic component in the structure is an organic fiber. In one embodiment, the mass reduction rate of the structure after heating at 1000° C. for 30 minutes in a nitrogen atmosphere is 1 mass % or more and less than 20 mass %. In one embodiment, inorganic particles are contained. In one embodiment, the inorganic particles include first inorganic particles that are non-layered particles and second inorganic particles that are layered particles. In one embodiment, the inorganic particles include first inorganic particles having a melting point of 1200°C or higher, and second inorganic particles having a melting point of less than 1200°C. In one embodiment, the maximum bending stress measured according to JIS K7017 is 9 MPa or more. In one embodiment, the bending strain at the maximum bending stress measured in accordance with JIS K7017 is 0.6% or more.
雖然專利文獻1中記載之結構體之成形性或形狀保持性較高,但關於兼顧提高鑄模製造時結構體之加工、組裝等操作性,減少於澆鑄時因源自結構體所包含之有機材料之燃燒氣體而導致之鑄物之氣體缺陷,及減少於鑄物表面產生之金屬滲透,仍有改善之餘地。Although the structure described in Patent Document 1 has high formability and shape retention, it is concerned with improving the workability of processing and assembling the structure at the time of casting mold production, and reducing the amount of organic materials contained in the structure during casting. There is still room for improvement in the gas defects of the castings caused by the combustion gases and the reduction of metal penetration on the surface of the castings.
因此,本發明係關於一種兼顧了提高操作性、減少氣體缺陷、及減少於鑄物表面產生之金屬滲透之鑄物製造用結構體。Therefore, the present invention relates to a structure for producing a cast product that achieves both improved workability, reduction of gas defects, and reduction of metal penetration on the surface of the cast product.
以下,基於其較佳之實施方式對本發明進行說明。 本發明之鑄物製造用結構體(以下,亦簡稱為「結構體」)適合用作用於鑄造之分割式模具或鑄模。 本說明書中,根據上下文,「鑄物製造用結構體」或「結構體」係指構成鑄模之一構件之構件、例如分割式模具、及鑄模本身。 關於本說明書中之「質量%」,只要無特別說明,則表示相對於鑄物製造用結構體之整體質量之質量比率。 Hereinafter, the present invention will be described based on its preferred embodiments. The structure for casting production of the present invention (hereinafter, also simply referred to as "structure") is suitably used as a split mold or casting mold for casting. In this specification, depending on the context, the "structure for casting production" or "structure" refers to a member constituting a member of a casting mold, for example, a split mold, and the casting mold itself. The "mass %" in this specification means the mass ratio with respect to the whole mass of the structure for casting manufacture unless otherwise specified.
以下說明中,為了便於說明,對未實施後述之塗佈等之鑄模之構成構件本身即鑄物製造用結構體進行說明。再者,於該結構體具有複數個構成構件、或由複數個層結構所形成之情形時,以下說明適用於任意構成構件或層結構。In the following description, for convenience of description, the structure body for casting product production, which is a constituent member of a casting mold to which coating or the like to be described later is not performed, will be described. In addition, when the structure has a plurality of constituent members or is formed of a plurality of layer structures, the following description applies to any constituent members or layer structures.
結構體較佳為包含有機纖維作為有機成分。有機纖維係包含有機成分之纖維狀物。由於有機纖維與後述之無機纖維相比更柔軟,故藉由該纖維彼此之相互纏繞、或與結構體中可含有之其他材料之結合,具有提高結構體之韌性之功能。 有機纖維較佳為至少分散存在於結構體之表面,更佳為分散存在於結構體之表面及內部。 藉由有機纖維分散存在於結構體之表面,於結構體表面形成纖維之網狀結構,與先前技術之結構體相比,可飛躍性地提高結構體之強度及韌性,防止由衝擊、彎曲、龜裂產生所導致之結構體之意外破裂或破壞。藉此,當將結構體切割加工為所需之長度時,可抑制龜裂產生或龜裂進展等結構體之破壞,即便於加工、組裝結構體時,亦可提高操作性,如不易產生破裂等。 The structure preferably contains organic fibers as an organic component. Organic fibers are fibrous substances containing organic components. Since the organic fibers are softer than the inorganic fibers described later, the fibers have the function of improving the toughness of the structure by intertwining the fibers with each other or bonding with other materials that may be contained in the structure. The organic fibers are preferably dispersed on at least the surface of the structure, and more preferably dispersed on the surface and inside of the structure. By dispersing the organic fibers on the surface of the structure, a network of fibers is formed on the surface of the structure. Compared with the structure of the prior art, the strength and toughness of the structure can be greatly improved, and the structure can be prevented from impact, bending, etc. Accidental rupture or destruction of a structure resulting from the occurrence of cracks. In this way, when the structural body is cut to a desired length, the damage of the structural body such as the occurrence of cracks or the progression of cracks can be suppressed, and the workability can be improved even when the structural body is processed and assembled. Wait.
本說明書中之所謂「有機成分」,係指於其分子結構中具有烴原子團之天然物或化合物。因此,僅由碳纖維等碳元素構成或包含碳元素及氮元素之材料不構成本發明中之有機成分及包含有機成分之材料。碳纖維被分類為後述之無機成分。The term "organic component" in this specification refers to a natural product or a compound having a hydrocarbon atomic group in its molecular structure. Therefore, a material composed of only carbon elements such as carbon fibers or containing carbon elements and nitrogen elements does not constitute the organic components and materials containing organic components in the present invention. Carbon fibers are classified into inorganic components to be described later.
結構體中是否包含有機成分可基於藉由固體NMR所得之對應於C=C鍵、C-H鍵、C=O鍵、O-H鍵之波峰之有無進行判定。該等鍵中,若至少存在C-H鍵或C=O鍵,則判定測定對象之材料包含有機成分。 又,結構體中是否包含有機纖維,可藉由上述固體NMR進行判定,並且可使用顯微FT-IR及顯微鏡(基恩士股份有限公司製造,型號:VHX-500,本說明書之顯微鏡全部為此種)觀察結構體之表面及內部而進行判定。詳細而言,於顯微FT-IR下確認源自有機物之官能基映射之位置,若利用顯微鏡於該位置觀察到有機纖維,則判定包含有機纖維。 Whether or not an organic component is included in the structure can be determined based on the presence or absence of peaks corresponding to C=C bonds, C-H bonds, C=O bonds, and O-H bonds obtained by solid-state NMR. Among these bonds, if there is at least a C-H bond or a C=O bond, it is determined that the material to be measured contains an organic component. In addition, whether or not the structure contains organic fibers can be determined by the above-mentioned solid-state NMR, and microscopic FT-IR and a microscope (manufactured by KEYENCE Co., Ltd., model: VHX-500, all microscopes in this specification are This) is judged by observing the surface and interior of the structure. In detail, the position where the functional group derived from the organic substance is mapped is confirmed by micro-FT-IR, and if organic fibers are observed at the position with a microscope, it is determined that organic fibers are included.
就更容易地形成有機纖維之網狀結構之觀點而言,結構體中之包含有機纖維之有機成分之含量以其總量計,較佳為大於5質量%,更佳為5.5質量%以上,進而較佳為6質量%以上。 就與上述相同之觀點而言,結構體中之有機纖維之含量較佳為0.3質量%以上,更佳為0.5質量%以上,進而較佳為1質量%以上。 From the viewpoint of easier formation of a network structure of organic fibers, the content of the organic components including organic fibers in the structure is preferably more than 5% by mass, more preferably 5.5% by mass or more, based on the total amount, More preferably, it is 6 mass % or more. From the same viewpoint as above, the content of the organic fibers in the structure is preferably 0.3% by mass or more, more preferably 0.5% by mass or more, and still more preferably 1% by mass or more.
又,就減少澆鑄時之氣體產生量之觀點而言,包含有機纖維之有機成分之含量以其總量計,較佳為未達20質量%,更佳為未達15質量%,進而較佳為未達13質量%。若為該等範圍,則可減少流入目標鑄物製品中之氣體,提高鑄物之品質。又,可抑制熔融金屬固著於源自結構體之有機成分熱分解後之部分等金屬滲透之不良情況。進而,可抑制於澆鑄過程中流入熔液時產生之氣體逆流而造成來自流入口端面之熔融金屬逆吹之情況,可提高澆鑄作業之安全性。 就與上述相同之觀點而言,結構體中之有機纖維之含量較佳為10質量%以下,更佳為5質量%以下,進而較佳為2.5質量%以下。 Also, from the viewpoint of reducing the amount of gas generated during casting, the content of the organic components including organic fibers is preferably less than 20% by mass, more preferably less than 15% by mass, and still more preferably was less than 13% by mass. Within these ranges, the gas flowing into the target casting product can be reduced, and the quality of the casting can be improved. Moreover, it is possible to suppress the inconvenience of metal penetration, such as the molten metal sticking to the part after the thermal decomposition of the organic component derived from the structure. Furthermore, it is possible to suppress the backflow of the molten metal from the end face of the inflow port due to the backflow of the gas generated when the molten metal flows in during the casting process, thereby improving the safety of the casting operation. From the same viewpoint as above, the content of the organic fibers in the structure is preferably 10% by mass or less, more preferably 5% by mass or less, and still more preferably 2.5% by mass or less.
關於鑄物製造用結構體之有機成分之含量,當對鑄物製造用結構體進行分析時,可依照以下順序進行測定。 作為預處理,對將成為測定對象之鑄物製造用結構體粉碎並均勻混合而成之樣品進行FT-IR分析。並且,藉由比較源自C=C鍵之波峰之檢測強度,定量結構體中所包含之碳纖維等僅由碳構成無機成分之含量進行。其後,將上述樣品於氮氣氛圍下,以1300℃以上之溫度加熱,使有機成分碳化,並且測定質量減少量。繼而,對碳化後之樣品進行FT-IR分析,定量殘存之碳成分之含量。最後,算出從碳化前樣品之碳成分之含量中減去碳化後樣品之碳成分之含量所得之值與質量減少量之合計值,將該合計值作為本發明中之有機成分之含量。 The content of the organic component in the structure for manufacturing a cast can be measured according to the following procedure when analyzing the structure for manufacturing a cast. As a pretreatment, FT-IR analysis was performed on a sample obtained by pulverizing and uniformly mixing the structure for manufacturing a casting to be measured. Furthermore, by comparing the detection intensities of the peaks derived from the C=C bond, the content of the inorganic components composed of only carbon such as carbon fibers contained in the structure was quantified. Then, the said sample was heated at the temperature of 1300 degreeC or more in nitrogen atmosphere, the organic component was carbonized, and the amount of mass loss was measured. Next, the carbonized sample was subjected to FT-IR analysis to quantify the content of the remaining carbon component. Finally, the total value of the value obtained by subtracting the carbon content of the sample after carbonization from the carbon content of the sample before carbonization and the amount of mass reduction are calculated, and the total value is used as the content of the organic component in the present invention.
有機纖維包括天然纖維、合成纖維、再生纖維、半合成纖維及回收纖維等。該等可單獨使用一種,或組合兩種以上使用。 天然纖維包括紙漿纖維、動物纖維等。 紙漿纖維包括木材紙漿、非木材紙漿等。 木材紙漿包括以針葉樹或闊葉樹為原料之機械紙漿、及以針葉樹或闊葉樹為原料之天然纖維素纖維等。 非木材紙漿包括棉紙漿、絨紙漿、麻、棉、竹、草、及以該等為原料之天然纖維素纖維等。 動物纖維包括羊毛、山羊毛、羊絨及羽毛等以蛋白質為主體之纖維。 Organic fibers include natural fibers, synthetic fibers, regenerated fibers, semi-synthetic fibers and recycled fibers. These can be used alone or in combination of two or more. Natural fibers include pulp fibers, animal fibers, and the like. Pulp fibers include wood pulp, non-wood pulp, and the like. Wood pulp includes mechanical pulp made from conifers or broad-leaved trees, and natural cellulose fibers made from conifers or broad-leaved trees. Non-wood pulp includes cotton pulp, lint pulp, hemp, cotton, bamboo, grass, and natural cellulose fibers using these as raw materials. Animal fibers include protein-based fibers such as wool, goat hair, cashmere, and feathers.
合成纖維例如可例舉包含聚烯烴樹脂、聚酯樹脂、聚醯胺樹脂、聚(甲基)丙烯酸樹脂、聚乙烯系樹脂、聚醯亞胺樹脂、芳香族聚醯胺樹脂等合成樹脂之纖維。該等樹脂可單獨使用,亦可組合複數種構成一根纖維。 作為聚烯烴樹脂,例如可例舉聚乙烯或聚丙烯等。 作為聚酯樹脂,例如可例舉聚對苯二甲酸乙二酯或聚對苯二甲酸丁二酯、聚萘二甲酸丁二酯、聚羥基丁酸酯、聚羥基烷酸酯、聚己內酯、聚丁二酸丁二酯、聚乳酸系樹脂等。 作為聚乳酸系樹脂,例如可例舉聚乳酸、乳酸-羥基羧酸共聚物等。 作為聚(甲基)丙烯酸樹脂,例如可例舉聚丙烯酸、聚甲基丙烯酸甲酯、聚丙烯酸酯、聚甲基丙烯酸、聚甲基丙烯酸酯等。 作為聚乙烯系樹脂,例如可例舉聚氯乙烯、聚偏二氯乙烯、乙酸乙烯酯樹脂、偏二氯乙烯樹脂、聚乙烯醇、聚乙烯醇縮乙醛、聚乙烯醇縮丁醛、聚苯乙烯等。 Examples of synthetic fibers include fibers containing synthetic resins such as polyolefin resins, polyester resins, polyamide resins, poly(meth)acrylic resins, polyethylene-based resins, polyimide resins, and aromatic polyamide resins. . These resins may be used alone or in combination to form one fiber. As a polyolefin resin, polyethylene, a polypropylene, etc. are mentioned, for example. As the polyester resin, for example, polyethylene terephthalate, polybutylene terephthalate, polybutylene naphthalate, polyhydroxybutyrate, polyhydroxyalkanoate, polycaprolactone may be mentioned. ester, polybutylene succinate, polylactic acid resin, etc. As a polylactic acid-type resin, a polylactic acid, a lactic acid-hydroxycarboxylic acid copolymer, etc. are mentioned, for example. As poly(meth)acrylic resin, polyacrylic acid, polymethyl methacrylate, polyacrylate, polymethacrylic acid, polymethacrylate, etc. are mentioned, for example. As the polyethylene-based resin, for example, polyvinyl chloride, polyvinylidene chloride, vinyl acetate resin, vinylidene chloride resin, polyvinyl alcohol, polyvinyl acetal, polyvinyl butyral, polyvinyl Styrene, etc.
作為再生纖維,例如可例舉銅氨纖維、嫘縈等。 作為半合成纖維,例如可例舉乙酸纖維等。 作為回收纖維,可例舉將廢紙、衣服等纖維類裁剪並開纖而得之紙漿纖維等。 該等之中,就提高結構體之韌性,提高操作性,於結構體製造時及鑄造時容易減少結構體表面之缺陷之觀點而言,較佳為使用紙漿纖維、包含聚酯樹脂之纖維及包含芳香族聚醯胺樹脂之纖維中之至少一種作為有機纖維。 As a regenerated fiber, cupro fiber, rayon, etc. are mentioned, for example. As a semi-synthetic fiber, cellulose acetate etc. are mentioned, for example. As recycled fibers, pulp fibers obtained by cutting and opening fibers such as waste paper and clothing can be mentioned. Among these, from the viewpoints of improving the toughness of the structure, improving the workability, and easily reducing the defects on the surface of the structure at the time of manufacture and casting of the structure, it is preferable to use pulp fibers, fibers containing polyester resin, and At least one of fibers containing an aromatic polyamide resin is used as the organic fiber.
就提高結構體之成形性並且提高操作性之觀點而言,較佳為結構體進而包含有機纖維以外之其他有機成分。 作為包含此種其他有機成分之材料,可例舉澱粉、熱硬化性樹脂、著色劑、熱膨脹性粒子等。該等可單獨使用一種,或組合兩種以上使用。 就抑制鑄造時結構體之燃燒,並且提高結構體之形狀保持性之觀點而言,較佳為使用熱硬化性樹脂。 From the viewpoint of improving the formability of the structure and improving the handleability, it is preferable that the structure further contains other organic components other than organic fibers. As a material containing such other organic components, starch, a thermosetting resin, a coloring agent, a heat-expandable particle, etc. are mentioned. These can be used alone or in combination of two or more. From the viewpoint of suppressing combustion of the structure during casting and improving the shape retention of the structure, it is preferable to use a thermosetting resin.
熱硬化性樹脂包括酚樹脂、改性酚樹脂、環氧樹脂、三聚氰胺樹脂、呋喃樹脂等。 酚樹脂包括酚醛型、可溶酚醛型等。 改性酚樹脂包括除酚以外還用脲、三聚氰胺及環氧樹脂等改性者。 該等可單獨使用一種,或組合兩種以上使用。 該等之中,就減少鑄造時之氣體產生,容易獲得尺寸穩定性或表面平滑性較高之鑄物之觀點而言,較佳為使用酚樹脂作為其他有機成分。 Thermosetting resins include phenol resins, modified phenol resins, epoxy resins, melamine resins, furan resins, and the like. Phenolic resins include novolac type, resol type, and the like. Modified phenol resins include those modified with urea, melamine and epoxy resin in addition to phenol. These can be used alone or in combination of two or more. Among these, it is preferable to use a phenol resin as the other organic component from the viewpoint of reducing gas generation during casting and easily obtaining a casting with high dimensional stability and surface smoothness.
結構體較佳為進而包含無機成分,更佳為進而包含無機粒子作為無機成分。藉由於結構體中含有無機成分,可提高結構體之耐熱性,提高澆鑄時之結構體之強度、尺寸穩定性及形狀維持性。 當結構體中包含無機粒子時,無機粒子較佳為至少存在於結構體之表面,更佳為同時存在於結構體之表面及內部。 當包含無機粒子時,無機粒子包括其熔點較佳為1200℃以上,進而較佳為1500℃以上者。藉由使用具有此種熔點之無機粒子,即便於澆鑄時之高溫條件下,結構體之形狀維持性亦優異。 無機粒子之熔點包括實際上為2500℃以下者。 若無機粒子之熔點處於上述範圍內,則於澆鑄時鑄物製造用結構體不會明顯熔解,可抑制鑄物之氣體缺陷或金屬滲透之產生。 The structure preferably further contains an inorganic component, and more preferably further contains inorganic particles as the inorganic component. By containing inorganic components in the structure, the heat resistance of the structure can be improved, and the strength, dimensional stability and shape retention of the structure during casting can be improved. When inorganic particles are included in the structure, the inorganic particles are preferably present at least on the surface of the structure, more preferably both on the surface and the interior of the structure. When inorganic particles are included, the inorganic particles include those whose melting point is preferably 1200°C or higher, more preferably 1500°C or higher. By using inorganic particles having such a melting point, the shape retention of the structure is excellent even under high temperature conditions during casting. The melting point of inorganic particles includes those that are actually 2500°C or lower. If the melting point of the inorganic particles is within the above-mentioned range, the structure for producing a cast product does not melt significantly during casting, and the occurrence of gas defects and metal penetration in the cast product can be suppressed.
藉由以下方法測定無機粒子之熔點。使用NIPPON STEEL TECHNOLOGY股份有限公司製造之示差熱天平-質量分析裝置(TG-DTA/MS),將鑄物製造用結構體於氮氣氛圍下從30℃以20℃/分鐘升溫至1500℃,經過30分鐘後,以20℃/分鐘冷卻至30℃,藉此進行測定。根據測定結果,判別鑄物製造用結構體中所含之無機成分之熔點。The melting point of the inorganic particles was measured by the following method. Using a differential thermal balance-mass analyzer (TG-DTA/MS) manufactured by NIPPON STEEL TECHNOLOGY Co., Ltd., the structure for casting production was heated from 30°C to 1500°C at 20°C/min under a nitrogen atmosphere, and the temperature was increased for 30 minutes. Minutes later, it measured by cooling to 30 degreeC at 20 degreeC/min. Based on the measurement results, the melting point of the inorganic component contained in the structure for manufacturing a cast is determined.
又,結構體較佳為包含選自如下化合物中之一種或兩種以上:選自鋁、鋯、矽及鐵元素中之元素之氧化物、碳化物及氮化物。即,結構體較佳為包含選自氧化鋁、二氧化矽、氧化鐵(II)、氧化鐵(III)、氮化鋁、氧化鋯、氮化矽、及碳化矽中之化合物之一種或兩種以上。 藉由於結構體中包含該等化合物,即便於澆鑄時之高溫條件下,亦會提高結構體之耐熱性,結構體之形狀維持性亦優異。 又,結構體中包含該等化合物,實質上意味著結構體中包含無機粒子。 結構體中包含上述化合物可藉由X射線繞射測定進行判定。作為具體之順序,藉由於管電壓30 KV、管電流15 mL、測角器掃描角度5~70°、測角器掃描速度10°/分鐘之條件下對測定對象之結構體進行測定,可判定上述化合物之有無及種類。 Moreover, it is preferable that the structure contains one or two or more compounds selected from the group consisting of oxides, carbides, and nitrides of elements selected from aluminum, zirconium, silicon, and iron. That is, the structure preferably contains one or two compounds selected from the group consisting of aluminum oxide, silicon dioxide, iron(II) oxide, iron(III) oxide, aluminum nitride, zirconium oxide, silicon nitride, and silicon carbide. more than one species. By including these compounds in the structure, the heat resistance of the structure is improved even under high temperature conditions during casting, and the shape retention of the structure is also excellent. In addition, the inclusion of these compounds in the structure essentially means that the structure includes inorganic particles. The inclusion of the above-mentioned compound in the structure can be determined by X-ray diffraction measurement. As a specific procedure, by measuring the structure of the object to be measured under the conditions of a tube voltage of 30 kV, a tube current of 15 mL, a goniometer scan angle of 5 to 70°, and a goniometer scan speed of 10°/min, it can be determined that The presence or absence and type of the above compounds.
除可具有上述熔點之無機粒子以外,還可包含黏土礦物。黏土礦物典型的是熔點未達1200℃者。 藉由進而使用具有此種熔點之無機粒子,於流入熔融金屬時黏土礦物熔融,可填充上述無機粒子間,防止無機粒子彼此之分離。其結果,可維持結構體之強度、形狀。 In addition to the inorganic particles which may have the above-mentioned melting point, clay minerals may also be contained. Clay minerals are typically those with a melting point of less than 1200°C. By further using inorganic particles having such a melting point, the clay minerals are melted when the molten metal is poured in, so that the inorganic particles can be filled between the inorganic particles and the inorganic particles can be prevented from being separated from each other. As a result, the strength and shape of the structure can be maintained.
無機粒子之形狀彼此獨立,可為球狀、多面體狀、鱗狀、層狀、紡錘狀、纖維狀、不定形、或該等之組合。 無機粒子可單獨使用一種,亦可組合兩種以上使用。 The shapes of the inorganic particles are independent of each other, and may be spherical, polyhedral, scaly, lamellar, fusiform, fibrous, amorphous, or a combination thereof. The inorganic particles may be used alone or in combination of two or more.
以下說明中,作為結構體中可包含之無機粒子,舉例說明使用第1無機粒子、第2無機粒子這兩種之情形。所謂第1無機粒子及第2無機粒子,特定之形狀及物性中之至少一個彼此不同。In the following description, as the inorganic particles that can be included in the structure, a case where both the first inorganic particle and the second inorganic particle are used will be exemplified. The first inorganic particles and the second inorganic particles are different from each other in at least one of specific shapes and physical properties.
一實施方式中之第1無機粒子較佳為非層狀粒子之粒子(即具有層狀以外之形狀之粒子)。又,一實施方式中之第2無機粒子較佳為層狀粒子。 另一實施方式中之第1無機粒子之熔點較佳為1200℃以上。又,另一實施方式中之第2無機粒子之熔點較佳為未達1200℃。 又一實施方式中之第1無機粒子之熔點較佳為1200℃以上且更佳為非層狀粒子之粒子。又,又一實施方式中之第2無機粒子之熔點較佳為未達1200℃且更佳為層狀粒子。如此,藉由使用複數種每個粒子具備複數個物性且各物性分別不同之無機粒子,可提高結構體之強度及操作性。 只要無特別說明,以下說明適當地適用於上述各實施方式中之說明。 The first inorganic particles in one embodiment are preferably non-layered particles (ie, particles having shapes other than layered). In addition, the second inorganic particles in one embodiment are preferably layered particles. The melting point of the first inorganic particles in another embodiment is preferably 1200° C. or higher. Moreover, it is preferable that the melting point of the 2nd inorganic particle in another embodiment is less than 1200 degreeC. The melting point of the first inorganic particles in another embodiment is preferably 1200° C. or higher, and more preferably non-layered particles. Moreover, it is preferable that the melting point of the 2nd inorganic particle in another embodiment is less than 1200 degreeC, and it is more preferable that it is a layered particle. In this way, by using a plurality of inorganic particles each having a plurality of physical properties and each of which is different from each other, the strength and handleability of the structure can be improved. Unless otherwise specified, the following descriptions are appropriately applied to the descriptions in each of the above-described embodiments.
關於第1無機粒子,就進而提高結構體之耐熱性之觀點而言,較佳為使用石墨、莫來石、黑曜石、鋯、氧化矽、飛灰及氧化鋁中之一種或兩種以上作為第1無機粒子,更佳為至少使用石墨及莫來石。莫來石中含有氧化鋁、二氧化矽及氧化鐵。 通常,石墨被分類為如鱗狀石墨或土狀石墨等天然生產之石墨,及以石油焦、碳黑或瀝青等為原料人工製造之人造石墨。該等石墨中,就提高結構體之成形性之觀點而言,較佳為使用鱗狀石墨。 Regarding the first inorganic particles, it is preferable to use one or more of graphite, mullite, obsidian, zirconium, silica, fly ash, and alumina as the first inorganic particles from the viewpoint of further improving the heat resistance of the structure. 1. Inorganic particles, preferably at least graphite and mullite are used. Mullite contains alumina, silica and iron oxide. Generally, graphite is classified into naturally produced graphite such as flake graphite or earthy graphite, and artificial graphite artificially produced from petroleum coke, carbon black or pitch, etc. Among these graphites, it is preferable to use scaly graphite from the viewpoint of improving the formability of the structure.
關於第1無機粒子之平均粒徑,就提高結構體之透氣性,抑制鑄物之氣體缺陷之觀點而言,較佳為1 μm以上,更佳為10 μm以上。 又,關於第1無機粒子之平均粒徑,就即便於澆鑄時結構體亦維持充分之熱強度之觀點而言,較佳為1000 μm以下,更佳為500 μm以下。 為了使無機粒子之平均粒徑處於上述範圍內,例如可篩分用作原料之無機粒子,或者可使用乾式粉碎或濕式粉碎等公知之粉碎裝置實施進一步粉碎處理。 The average particle diameter of the first inorganic particles is preferably 1 μm or more, more preferably 10 μm or more, from the viewpoint of improving the air permeability of the structure and suppressing gas defects in the casting. In addition, the average particle diameter of the first inorganic particles is preferably 1000 μm or less, more preferably 500 μm or less, from the viewpoint of maintaining a sufficient thermal strength of the structure even during casting. In order to keep the average particle diameter of the inorganic particles within the above range, for example, the inorganic particles used as raw materials can be sieved, or further pulverization can be performed using a known pulverizing device such as dry pulverization or wet pulverization.
第1無機粒子之平均粒徑可藉由例如使用雷射繞射/散射式粒徑分佈測定裝置(LA-950V2,堀場製作所股份有限公司製造)測定粒徑分佈而得到。粒徑分佈之測定係使用乾式單元作為附件,測定無機粒子因壓縮空氣而分散之粉末狀態之粒徑。測定條件為將壓縮空氣之壓力設為0.20 MPa,流量設為320 L/分鐘,可調整投入量,使雷射之吸光度為95%~99%,而對試樣進行測定。由所得之體積基準之粒徑分佈算出粒徑之中值,將其定義為平均粒徑。The average particle size of the first inorganic particles can be obtained by measuring the particle size distribution using, for example, a laser diffraction/scattering particle size distribution analyzer (LA-950V2, manufactured by HORIBA, Ltd.). The particle size distribution is measured by using a dry cell as an accessory to measure the particle size of the inorganic particles in a powder state dispersed by compressed air. The measurement conditions are that the pressure of the compressed air is set to 0.20 MPa, the flow rate is set to 320 L/min, and the input amount can be adjusted so that the absorbance of the laser is 95% to 99%, and the sample is measured. From the obtained volume-based particle size distribution, the median value of the particle size was calculated and defined as the average particle size.
於包含第2無機粒子作為無機粒子之情形時,第2無機粒子較佳為層狀黏土礦物。即,較佳為結構體包含層狀粒子作為第2無機粒子,更佳為包含黏土礦物之層狀粒子。 由於層狀黏土礦物因含有水而膨潤,可獲得增黏效果,故於製造結構體時該結構體之各原料容易均勻地混合。又,於乾燥時,層狀黏土礦物失去於其單位結晶層間存在之水分子,無機粒子及有機纖維一面形成緊密之結構一面固化,藉此提高常溫時之該結構體之強度之同時可提高操作性,並且可有效地賦予鑄物製造時之熱強度。除此之外,可維持結構體之加工性及形狀保持性,並且製造之鑄物之表面平滑性較高,可減少氣體缺陷之產生率。 When the second inorganic particles are included as the inorganic particles, the second inorganic particles are preferably layered clay minerals. That is, the structure preferably contains layered particles as the second inorganic particles, and more preferably contains layered particles of clay minerals. Since the layered clay minerals swell due to the inclusion of water, the viscosity-increasing effect can be obtained, so the raw materials of the structure are easily mixed uniformly when the structure is manufactured. In addition, during drying, the layered clay minerals lose the water molecules existing between the unit crystal layers, and the inorganic particles and organic fibers form a compact structure while solidifying, thereby increasing the strength of the structure at room temperature and improving the handling. properties, and can effectively impart thermal strength to the casting. In addition, the workability and shape retention of the structure can be maintained, and the surface smoothness of the produced casting can be high, and the occurrence rate of gas defects can be reduced.
就製作出兼具結構體之耐熱性及強度,於結構體製造時、操作時及使用該結構體澆鑄時,操作性、尺寸穩定性及形狀維持性優異之結構體之觀點而言,作為無機粒子,較佳為組合使用球狀粒子與層狀粒子。更詳細而言,作為無機粒子,較佳為組合使用球狀粒子等非層狀粒子之第1無機粒子、及作為層狀粒子之第2無機粒子之層狀黏土礦物粒子。 為了確認結構體中包含球狀粒子及層狀粒子,可藉由使用掃描式電子顯微鏡(SEM)於結構體之表面觀察粒子之形狀來進行判定。 From the viewpoint of producing a structure having both heat resistance and strength of the structure, and excellent workability, dimensional stability, and shape retention during the production, handling, and casting of the structure, as an inorganic As for the particles, spherical particles and layered particles are preferably used in combination. More specifically, as the inorganic particles, it is preferable to use a combination of the first inorganic particles that are non-layered particles such as spherical particles, and the layered clay mineral particles that are the second inorganic particles that are layered particles. In order to confirm that spherical particles and layered particles are included in the structure, it can be determined by observing the shape of the particles on the surface of the structure using a scanning electron microscope (SEM).
可用作第2無機粒子之層狀黏土礦物主要藉由層狀黏土礦物介於有機纖維或其他材料之間而具有賦予結構體成形性,進而提高常溫強度及熱強度之功能。 作為層狀黏土礦物,可使用以層狀矽酸鹽礦物為代表之具有層狀結構之結晶性之無機化合物。層狀黏土礦物可為天然者,亦可為人工製造者。 The layered clay minerals that can be used as the second inorganic particles have the function of imparting formability to the structure by interposing the layered clay minerals between organic fibers or other materials, thereby improving the strength at room temperature and thermal strength. As the layered clay mineral, a crystalline inorganic compound having a layered structure represented by a layered silicate mineral can be used. Layered clay minerals can be natural or artificial.
作為層狀黏土礦物之具體例,可例舉以高嶺石族、膨潤石族及雲母族等為代表之黏土礦物。該等各種層狀黏土礦物可單獨或組合兩種以上使用。 作為高嶺石族之黏土礦物,例如可例舉高嶺石。作為膨潤石族之黏土礦物,例如可例舉蒙脫石、膨潤土、皂石、鋰膨潤石、鋁膨潤石、矽鎂石及綠脫石等。 作為雲母族之黏土礦物,例如可例舉蛭石、多水高嶺土及四矽雲母(tetra silicic mica)等。 此外,亦可使用作為層狀雙氫氧化物之鋁碳酸鎂等。 上述層狀黏土礦物中,蒙脫石或膨潤土於含水狀態下與各成分之黏結力較強,就製造結構體時之成形時之形狀賦予性之觀點而言適合使用。 又,就澆鑄時之耐熱性之觀點而言,適合使用高嶺石或蒙脫石。 Specific examples of the layered clay minerals include clay minerals represented by the kaolinite group, the bentonite group, and the mica group. These various layered clay minerals may be used alone or in combination of two or more. As a clay mineral of the kaolinite family, for example, kaolinite can be mentioned. Examples of the clay minerals of the bentonite family include montmorillonite, bentonite, saponite, lithium bentonite, aluminum bentonite, stevensite, and nontronite. As a clay mineral of mica group, vermiculite, halloysite, tetra silicic mica, etc. are mentioned, for example. Moreover, aluminum magnesium carbonate etc. can also be used as a layered double hydroxide. Among the above-mentioned layered clay minerals, montmorillonite or bentonite has a strong binding force with each component in a water-containing state, and is suitable for use from the viewpoint of shape imparting properties at the time of molding when producing a structure. Moreover, from the viewpoint of heat resistance at the time of casting, kaolinite or montmorillonite is suitably used.
關於第2無機粒子之平均粒徑,就提高結構體之透氣性而抑制鑄物之氣體缺陷之觀點而言,較佳為0.1 μm以上,更佳為1 μm以上。 就提高結構體之強度、成形性及保形性之觀點而言,第2無機粒子之平均粒徑較佳為500 μm以下,更佳為200 μm以下。 於使用層狀黏土礦物作為第2無機粒子之情形時,可使層狀黏土礦物之平均粒徑處於上述範圍內。 第2無機粒子之平均粒徑可藉由與上述第1無機粒子之平均粒徑之測定方法相同之方法進行測定。 The average particle diameter of the second inorganic particles is preferably 0.1 μm or more, more preferably 1 μm or more, from the viewpoint of improving the air permeability of the structure and suppressing gas defects in the casting. From the viewpoint of improving the strength, formability, and shape retention of the structure, the average particle diameter of the second inorganic particles is preferably 500 μm or less, more preferably 200 μm or less. When the layered clay mineral is used as the second inorganic particles, the average particle diameter of the layered clay mineral can be within the above-mentioned range. The average particle diameter of the second inorganic particles can be measured by the same method as the method for measuring the average particle diameter of the first inorganic particles described above.
結構體於鑄造時等之高溫環境下之質量減少率處於特定範圍內。結構體之質量減少率與於鑄造時因結構體中之有機成分而產生之氣體產生率存在關聯。具體而言,呈現質量減少率越低,則氣體產生率越低之傾向。 因此,質量減少率越少,則意味著越可更加穩定地維持結構體之熱強度,並且於維持製造之鑄物之尺寸精度、或減少由於澆鑄中產生之氣體混入鑄物製品中而導致之氣體缺陷及減少結構體對鑄物表面之金屬滲透之方面優異。 The mass reduction rate of the structure in a high temperature environment such as casting is within a specific range. The mass reduction rate of the structure correlates with the gas generation rate due to the organic components in the structure during casting. Specifically, the lower the mass reduction rate, the lower the gas generation rate tends to be. Therefore, the smaller the mass reduction rate, the more stably the thermal strength of the structure can be maintained, and the dimensional accuracy of the manufactured casting can be maintained, or the reduction of the gas generated during casting. Excellent in gas defects and reduction of metal penetration of the structure to the casting surface.
詳細而言,結構體於氮氣氛圍下以1000℃加熱30分鐘後之質量減少率較佳為未達20%,更佳為未達15質量%,進而較佳為未達9質量%。若質量減少率為該範圍,則於澆鑄過程中流入高溫熔液時產生之氣體量會降低,流入鑄物製品中之氣體會減少,因此鑄物之品質會進而提高。又,可抑制熔融金屬固著於源自結構體之有機成分熱分解後之部分等金屬滲透之不良情況。進而,可抑制於澆鑄過程中流入熔液時產生之氣體逆流而造成來自流入口端面之熔融金屬逆吹之情況,可提高澆鑄作業之安全性。 又,為了有效地達成氣體產生率之減少,上述質量減少率越低越佳,但是就充分地達成防止由於有機纖維提高結構體之韌性而導致之結構體之崩解之觀點而言,較佳為1質量%以上,更佳為3質量%以上,進而較佳為大於5質量%。 為了達成該等質量減少率,例如可將包含有機纖維之有機成分或各無機粒子之含量設為上述適宜之範圍,或者於結構體之製造步驟中之成形後進行熱處理,進行氣體產生成分之去除處理。 Specifically, the mass reduction rate of the structure after heating at 1000° C. for 30 minutes under a nitrogen atmosphere is preferably less than 20%, more preferably less than 15% by mass, and still more preferably less than 9% by mass. If the mass reduction rate is within this range, the amount of gas generated when the high-temperature melt flows in the casting process will be reduced, and the gas flowing into the cast product will be reduced, so the quality of the cast will be further improved. Moreover, it is possible to suppress the inconvenience of metal penetration, such as the molten metal sticking to the part after the thermal decomposition of the organic component derived from the structure. Furthermore, it is possible to suppress the backflow of the molten metal from the end face of the inflow port due to the backflow of the gas generated when the molten metal flows in during the casting process, thereby improving the safety of the casting operation. In addition, in order to effectively reduce the gas generation rate, the above-mentioned mass reduction rate is preferably as low as possible, but from the viewpoint of sufficiently preventing the disintegration of the structure due to the increase in the toughness of the organic fiber, it is preferable. It is 1 mass % or more, More preferably, it is 3 mass % or more, More preferably, it is more than 5 mass %. In order to achieve such a mass reduction rate, for example, the content of the organic component including organic fibers or each inorganic particle can be set to the above-mentioned suitable range, or the gas generating component can be removed by heat treatment after forming in the production step of the structure. deal with.
關於質量減少率,使用熱重量測定裝置(Seiko Instruments股份有限公司製造,STA7200RV TG/DTA),於氮氣氛圍下將測定對象之鑄物製造用結構體從30℃以升溫速度20℃/分鐘加熱至1000℃,於1000℃下維持30分鐘。此時,以30℃下結構體之質量為基準(100%),測定1000℃下質量之變化作為溫度之函數,以1000℃下結構體之質量相對於30℃下結構體之質量之百分率之形式算出質量減少率(%)。Regarding the mass reduction rate, a thermogravimetric measuring apparatus (manufactured by Seiko Instruments Co., Ltd., STA7200RV TG/DTA) was used to heat the structure to be measured from 30°C at a temperature increase rate of 20°C/min to 20°C/min under nitrogen atmosphere. 1000°C for 30 minutes at 1000°C. At this time, based on the mass of the structure at 30°C (100%), the change in mass at 1000°C was measured as a function of temperature, and the percentage of the mass of the structure at 1000°C relative to the mass of the structure at 30°C was calculated. The mass reduction rate (%) was calculated in the form.
關於結構體,作為結構體具有之韌性之指標之一測定之最大彎曲應力較佳為9 MPa以上,更佳為12 MPa以上。藉由具有該等最大彎曲應力,可成為韌性較高之結構體,防止結構體之崩解或破裂、龜裂之產生,提高結構體之操作性、形狀維持性及尺寸穩定性。 又,關於結構體之最大彎曲應力,就兼顧提高結構體之操作性及澆鑄時之操作性之觀點而言,較佳為50 MPa以下,更佳為40 MPa以下,進而較佳為30 MPa以下。 Regarding the structure, the maximum bending stress measured as one of the indicators of the toughness possessed by the structure is preferably 9 MPa or more, more preferably 12 MPa or more. By having these maximum bending stresses, a structure with high toughness can be obtained, disintegration, cracking, and cracking of the structure can be prevented, and the handleability, shape retention, and dimensional stability of the structure can be improved. In addition, the maximum bending stress of the structure is preferably 50 MPa or less, more preferably 40 MPa or less, and still more preferably 30 MPa or less, from the viewpoint of improving both the workability of the structure and the workability at the time of casting. .
又,關於結構體,作為結構體具有之韌性之指標之一測定之最大彎曲應力時之彎曲應變(以下,亦簡稱為「彎曲應變」)較佳為0.6%以上,更佳為0.65%以上。藉由具有該等彎曲應變,可成為韌性較高之結構體,防止結構體之崩解或破裂、龜裂之產生,提高結構體之操作性、形狀維持性及尺寸穩定性。 又,雖然結構體之彎曲應變越大越佳,但實際上較佳為8%以下,更佳為6%以下,進而較佳為4%以下。 In addition, about the structure, the bending strain at the maximum bending stress (hereinafter, also simply referred to as "bending strain") measured as one of the indicators of the toughness of the structure is preferably 0.6% or more, more preferably 0.65% or more. By having these bending strains, a structure with high toughness can be obtained, the disintegration or cracking of the structure, and the occurrence of cracks can be prevented, and the handleability, shape retention and dimensional stability of the structure can be improved. In addition, although the bending strain of the structure is preferably as large as possible, it is actually preferably 8% or less, more preferably 6% or less, and still more preferably 4% or less.
結構體之彎曲應變及最大彎曲應力可使用測定裝置(島津製作所股份有限公司製造,萬能試驗機AGX-plus),依據JIS K7017之三點彎曲試驗而進行測定。此時,作為測定試樣之結構體係切割出具有縱60 mm×橫15 mm×厚2 mm之板狀之樣品進行測定。 最大彎曲應力係將於三點彎曲試驗時賦予樣品之力矩(負載與距離之積)除以樣品之剖面係數而算出之物性值。於無法由作為測定對象之結構體之尺寸切割出上述板狀之樣品之情形時,可切割出具有任意尺寸之樣品進行測定。 The bending strain and the maximum bending stress of the structure can be measured according to the three-point bending test of JIS K7017 using a measuring device (manufactured by Shimadzu Corporation, universal testing machine AGX-plus). At this time, as the structural system of the measurement sample, a plate-shaped sample having a length of 60 mm × a width of 15 mm × a thickness of 2 mm was cut out for measurement. The maximum bending stress is the physical property value calculated by dividing the moment (the product of the load and the distance) imparted to the sample by the section coefficient of the sample during the three-point bending test. When the above-mentioned plate-shaped sample cannot be cut out from the size of the structure to be measured, a sample having an arbitrary size can be cut out for measurement.
關於具有以上構成之鑄物製造用結構體,由於含有有機纖維,有機纖維具有適度之柔軟性或彈性,故可提高有機纖維彼此、或者有機纖維與其他材料之相互纏繞性或結合性,提高結構體之韌性。其結果,對脆性破壞之抵抗性提高,即便於製造結構體時,或輸送、加工、組裝等操作時,或者澆鑄過程中之高溫負載時等各情形時,亦可抑制結構體表面或內部之崩解缺損或龜裂、破裂之產生,提高結構體之操作性。又,亦可防止於澆鑄時成為熔融金屬流入鑄模時之流路之澆注口之意外崩解或斷裂。尤其是,由於有機纖維存在於結構體之表面,故有機纖維彼此相互纏繞形成網狀結構,承擔如覆蓋結構體之網之作用,因此可有效地抑制結構體表面之崩解缺損或龜裂、破裂之產生。The structure for cast production having the above constitution contains organic fibers, and the organic fibers have moderate flexibility or elasticity, so that the entanglement or bonding between organic fibers or between organic fibers and other materials can be improved, and the structure can be improved. Resilience of the body. As a result, the resistance to brittle failure is improved, and even in the case of manufacturing the structure, or during operations such as transportation, processing, and assembly, or under high temperature load during casting, the surface or interior of the structure can be suppressed. Disintegration defects or cracks and cracks occur, and the operability of the structure is improved. In addition, accidental disintegration or breakage of the sprue, which becomes a flow path for molten metal flowing into the mold during casting, can also be prevented. In particular, since the organic fibers exist on the surface of the structure, the organic fibers are intertwined with each other to form a network structure, which acts as a net covering the structure, so it can effectively suppress the disintegration defect or cracking of the surface of the structure. The occurrence of rupture.
又,即便於製造結構體時,輸送、加工、組裝等操作時,或者於澆鑄時意外產生微小之龜裂或崩解等缺陷之情形時,由於存在有機纖維之網狀結構,故亦可抑制龜裂等缺陷之進一步之進展,結構體可表現出較高之形狀保持性。 進而,藉由使結構體中含有無機粒子,成為具有可耐受鑄造之較高之耐熱性者。作為無機粒子之適宜之形態,組合使用黏土礦物以外之材料與黏土礦物,藉此結構體之耐熱性優異,結構體會表現出較高之常溫強度及熱強度,並且兼具因源於有機纖維之高韌性而產生之結構體之優異操作性。 除此之外,藉由將結構體之質量減少率控制於特定範圍,於將該結構體用作鑄模進行澆鑄時,可有效地減少結構體對鑄物表面之金屬滲透、或氣體缺陷等鑄物缺陷。其結果,可製造尺寸精度或表面平滑性優異之鑄物,並且可降低鑄物之製造成本。 In addition, even in the case of manufacturing the structure, during transportation, processing, assembly, etc., or in the case of accidental occurrence of small cracks or disintegration defects during casting, due to the presence of the network structure of organic fibers, it can be suppressed. With the further development of defects such as cracks, the structure can exhibit higher shape retention. Furthermore, by containing inorganic particles in the structure, it becomes one with high heat resistance that can withstand casting. As a suitable form of inorganic particles, materials other than clay minerals and clay minerals are used in combination, whereby the structure has excellent heat resistance, the structure exhibits high normal temperature strength and thermal strength, and has both properties derived from organic fibers. Excellent handleability of structures resulting from high toughness. In addition, by controlling the mass reduction rate of the structure within a specific range, when the structure is used as a mold for casting, it is possible to effectively reduce the metal penetration of the structure to the surface of the casting, or the casting of gas defects. material defect. As a result, a cast product excellent in dimensional accuracy and surface smoothness can be produced, and the production cost of the cast product can be reduced.
對於結構體,亦要求提高其加工時或組裝時之操作性,於結構體之韌性較低之情形時,於將結構體切割為特定尺寸等加工時,結構體中容易形成皸裂或缺漏、破裂等缺陷部分。關於容易產生該等缺陷部分之結構體,將其用於澆鑄時結構體本身會從缺陷部分開始崩解,或者熔融金屬會滲出至結構體外。其結果,該等結構體之操作性較差,同時鑄造效率亦較差。For the structure, it is also required to improve the operability during processing or assembly. When the toughness of the structure is low, when the structure is cut into a specific size, cracks, omissions, or cracks are easily formed in the structure. and other defective parts. With regard to a structure that is prone to such defective parts, when it is used for casting, the structure itself disintegrates from the defective part, or molten metal oozes out of the structure. As a result, the operability of these structures is poor, and the casting efficiency is also poor.
關於該點,由於本發明之結構體具有韌性優異之構成,故可利用切割器等簡便地切割本結構體以調整尺寸並使用,又,即便於進行切割處理時,亦不易於結構體中形成皸裂或缺漏、破裂等缺陷部分。進而,即便於連接複數個結構體、或者使用複數個結構體組裝成一個鑄模時,亦不易於各結構體中形成皸裂或缺漏、破裂等缺陷部分。其結果,本發明之結構體於加工時或組裝時之操作性優異。In this regard, since the structure of the present invention has a structure excellent in toughness, the structure can be easily cut with a cutter or the like to adjust the size and use, and it is not easy to form in the structure even when the cutting process is performed. Defective parts such as chapped or missing, cracked, etc. Furthermore, even when a plurality of structures are connected or assembled into one mold using a plurality of structures, it is difficult to form defective parts such as cracks, omissions, and cracks in each of the structures. As a result, the structure of the present invention is excellent in workability during processing or assembly.
就提高結構體之韌性,進而有效地抑制結構體表面之崩解缺損或龜裂、破裂之產生,提高使用時之操作性之觀點而言,結構體較佳為有機纖維存在於結構體之表面,又,結構體表面之每單位面積之有機纖維之根數較佳為特定值以上。 詳細而言,結構體中,有機纖維於結構體之表面每100 mm 2內較佳為存在50根以上,更佳為存在70根以上,進而較佳為存在100根以上。 又,於結構體之表面每100 mm 2內存在之有機纖維之根數實際上為300根以下。 From the viewpoint of improving the toughness of the structure, thereby effectively suppressing the occurrence of disintegration defects, cracks and cracks on the surface of the structure, and improving the operability during use, the structure is preferably organic fibers present on the surface of the structure. , and the number of organic fibers per unit area on the surface of the structure is preferably a specific value or more. Specifically, in the structure, there are preferably 50 or more organic fibers per 100 mm 2 on the surface of the structure, more preferably 70 or more, and still more preferably 100 or more. In addition, the number of organic fibers present per 100 mm 2 on the surface of the structure is actually 300 or less.
關於存在於結構體表面之有機纖維之根數,首先,藉由使用上述固體NMR、顯微FT-IR及顯微鏡之方法判定存在於結構體表面之纖維狀物為有機纖維。其後,可對利用顯微鏡或SEM觀察包含有機纖維之結構體表面而得之纖維觀察圖像資料使用圖像處理軟體(三谷商事股份有限公司製造,WinROOF,本說明書之圖像處理軟體全部為此種),將100 mm 2之面積作為1視野,算出測定3視野以上時之根數之算術平均值。 測定有機纖維之根數時,對於成為測定對象之面積,可一次觀察100 mm 2之面積,或者亦可將觀察次數分為複數次觀察100 mm 2之面積,例如觀察10次10 mm 2之面積等。 Regarding the number of organic fibers existing on the surface of the structure, first, the fibrous substances existing on the surface of the structure were determined to be organic fibers by the methods using the above-mentioned solid-state NMR, microscopic FT-IR and microscope. After that, the fiber observation image data obtained by observing the surface of the structure containing organic fibers with a microscope or SEM can use image processing software (manufactured by Sangu Shoji Co., Ltd., WinROOF, all the image processing software in this manual are for this purpose. species), the area of 100 mm 2 was regarded as 1 field of view, and the arithmetic mean of the number of roots when measuring 3 or more fields of view was calculated. When measuring the number of organic fibers, for the area to be measured, an area of 100 mm2 can be observed at one time, or the number of observations can be divided into multiple times to observe an area of 100 mm2 , for example, an area of 10 mm2 can be observed 10 times. Wait.
就容易使複數個其他纖維或材料與單根纖維接觸,提高纖維彼此之相互纏繞性或與其他材料之結合性,進而提高結構體之韌性,提高結構體之操作性之觀點而言,存在於結構體表面之有機纖維之平均纖維長度L1較佳為0.5 mm以上,進而較佳為1 mm以上。 就提高製造結構體時之成形性,及提高製造時及澆鑄時之結構體之尺寸均勻性之觀點而言,存在於結構體表面之有機纖維之平均纖維長度L1較佳為7 mm以下,更佳為5 mm以下,進而較佳為4 mm以下。 關於有機纖維之平均纖維長度L1,可利用顯微鏡或SEM觀察結構體表面而獲得纖維觀察圖像資料,使用圖像處理軟體,以50根纖維為對象,測定出測定對象之纖維之一端至另一端之長度,將其等之算術平均值作為平均纖維長度。 From the point of view of easily contacting a plurality of other fibers or materials with a single fiber, improving the mutual entanglement of fibers or bonding with other materials, thereby improving the toughness of the structure, and improving the operability of the structure. The average fiber length L1 of the organic fibers on the surface of the structure is preferably 0.5 mm or more, more preferably 1 mm or more. The average fiber length L1 of the organic fibers present on the surface of the structure is preferably 7 mm or less, from the viewpoint of improving the formability of the structure during manufacture and improving the dimensional uniformity of the structure during manufacture and casting. It is preferably 5 mm or less, and more preferably 4 mm or less. Regarding the average fiber length L1 of the organic fibers, the fiber observation image data can be obtained by observing the surface of the structure with a microscope or SEM. Using image processing software, 50 fibers are used as the object, and one end to the other end of the fiber to be measured is measured. The arithmetic mean of the lengths was taken as the average fiber length.
就由於纖維之表面積之增加而增加與其他纖維或材料之接觸面積,提高纖維彼此之相互纏繞性、或與其他材料之結合性,進而提高結構體之韌性,提高結構體之操作性之觀點而言,存在於結構體表面之有機纖維之平均纖維直徑D1較佳為8 μm以上,更佳為10 μm以上。 就提高製造結構體時之成形性,及提高製造時及澆鑄時之結構體之尺寸均勻性之觀點而言,存在於結構體表面之有機纖維之平均纖維直徑D1較佳為未達40 μm,更佳為未達35 μm,進而較佳為30 μm以下。 關於有機纖維之平均纖維直徑D1,可利用顯微鏡或SEM觀察結構體表面而獲得纖維觀察圖像資料,使用圖像處理軟體,以任意選出之50根纖維為對象,對每根纖維測定5處與測定對象之纖維之長度方向正交之長度,將此時之算術平均值作為平均纖維直徑。 In terms of increasing the contact area with other fibers or materials due to the increase in the surface area of the fibers, improving the mutual entanglement of fibers or bonding with other materials, thereby improving the toughness of the structure, and improving the operability of the structure. In other words, the average fiber diameter D1 of the organic fibers present on the surface of the structure is preferably 8 μm or more, more preferably 10 μm or more. The average fiber diameter D1 of the organic fibers present on the surface of the structure is preferably less than 40 μm from the viewpoint of improving the formability at the time of manufacturing the structure and improving the dimensional uniformity of the structure at the time of manufacturing and casting. More preferably, it is less than 35 μm, and still more preferably 30 μm or less. Regarding the average fiber diameter D1 of the organic fibers, the fiber observation image data can be obtained by observing the surface of the structure with a microscope or SEM. Using image processing software, 50 fibers selected at random are used as the object, and 5 positions of the fiber are measured for each fiber. The length perpendicular to the longitudinal direction of the fiber to be measured was measured, and the arithmetic mean value at that time was taken as the average fiber diameter.
就提高纖維彼此之相互纏繞性或與其他材料之結合性,進而提高結構體之剛性及強度之觀點而言,存在於結構體之表面之有機纖維之平均纖維長度(單位:mm)相對於平均纖維直徑(單位:mm)之比,即,平均纖維長度L1(單位:mm)除以平均纖維直徑D1(單位:μm)以1000除得之值之比即「1000×平均纖維長度L1/平均纖維直徑D1」之比較佳為10以上,更佳為30以上,進而較佳為50以上,特佳為100以上。 就提高製造結構體時之成形性、及提高製造時及澆鑄時之結構體之尺寸均勻性之觀點而言,「1000×平均纖維長度L1/平均纖維直徑D1」之比較佳為260以下,進而較佳為230以下。 From the viewpoint of improving the mutual entanglement of fibers or bonding with other materials, thereby improving the rigidity and strength of the structure, the average fiber length (unit: mm) of the organic fibers existing on the surface of the structure is relative to the average fiber length (unit: mm). The ratio of the fiber diameter (unit: mm), that is, the ratio of the value obtained by dividing the average fiber length L1 (unit: mm) by the average fiber diameter D1 (unit: μm) divided by 1000 is “1000×average fiber length L1/average The ratio of the fiber diameter D1" is preferably 10 or more, more preferably 30 or more, still more preferably 50 or more, and particularly preferably 100 or more. From the viewpoint of improving the formability at the time of manufacturing the structure and improving the dimensional uniformity of the structure at the time of manufacture and casting, the ratio of “1000×average fiber length L1/average fiber diameter D1” is preferably 260 or less, and further Preferably it is 230 or less.
於發揮本發明之效果之範圍內,鑄物製造用結構體可進而包含無機纖維。 於包含無機纖維之情形時,無機纖維主要具有於製造時及鑄造時維持結構體之形狀而不燃燒之功能。 可使用之無機纖維包括人造礦物纖維、陶瓷纖維、及天然礦物纖維等。 人造礦物纖維包括PAN(Polyacrylonitrile,聚丙烯腈)系碳纖維及瀝青系碳纖維等碳纖維、及岩絨等。 該等無機纖維可單獨或組合兩種以上使用。 該等之中,就於澆鑄時之高溫環境下維持結構體之形狀及強度之觀點而言,較佳為使用碳纖維。 碳纖維係於結構中無烴原子團,並且於結構中含有碳雙鍵之纖維。碳纖維典型的是僅由碳元素構成。 In the range where the effect of this invention is exhibited, the structure for casting manufacture may further contain an inorganic fiber. In the case of including inorganic fibers, the inorganic fibers mainly have the function of maintaining the shape of the structure without burning during manufacture and casting. Inorganic fibers that can be used include man-made mineral fibers, ceramic fibers, and natural mineral fibers. Man-made mineral fibers include carbon fibers such as PAN (Polyacrylonitrile, polyacrylonitrile)-based carbon fibers and pitch-based carbon fibers, rock wool, and the like. These inorganic fibers may be used alone or in combination of two or more. Among them, carbon fibers are preferably used from the viewpoint of maintaining the shape and strength of the structure in a high-temperature environment at the time of casting. Carbon fibers are fibers that have no hydrocarbon radicals in their structure and contain carbon double bonds in their structure. Carbon fibers are typically composed of only carbon elements.
結構體中是否包含無機纖維可藉由以下方法來判定。 首先,以存在於結構體表面之纖維狀物為對象,藉由掃描式電子顯微鏡(SEM)-能量色散型X射線光譜(EDX)分析法或進行顯微FT-IR分析而進行元素映射及元素分析。根據該等分析,進行纖維狀物中之含有元素之種類、分子鍵之種類及量之分析。根據該等分析,於觀測到包含C=C鍵之纖維狀物且該纖維狀物不同時包含金屬元素及氧元素,或者觀測到不包含C-H鍵、C=O鍵、O-H鍵之纖維狀物之情形時,判定該纖維狀物為無機纖維。 Whether or not inorganic fibers are included in the structure can be determined by the following method. First, elemental mapping and elemental mapping by scanning electron microscopy (SEM)-energy dispersive X-ray spectroscopy (EDX) analysis or microscopic FT-IR analysis are carried out on the fibrous objects existing on the surface of the structure as objects. analyze. Based on these analyses, the types of elements and the types and amounts of molecular bonds contained in the fibrous material were analyzed. According to these analyses, fibers containing C=C bonds are observed and the fibers do not contain both metal elements and oxygen elements, or fibers that do not contain C-H bonds, C=O bonds, and O-H bonds are observed. In this case, it is determined that the fibrous material is an inorganic fiber.
於結構體包含無機纖維之情形時,就提高鑄物製造用結構體之成形性及均勻性之觀點而言,無機纖維之平均纖維長度較佳為0.5 mm以上,更佳為1 mm以上。 又,關於無機纖維之平均纖維長度,就提高結構體之成形性之觀點而言,較佳為15 mm以下,更佳為8 mm以下,進而較佳為5 mm以下。 關於無機纖維之平均纖維長度,首先,以存在於結構體表面之纖維狀物為對象,藉由上述方法判定及特定出作為無機纖維之纖維狀物。其後,從利用顯微鏡或SEM於倍率50倍下以無機纖維為對象進行顯微鏡觀察時之二維畫面中,任意選出30根以上之纖維,以此為對象,測定一端至另一端之長度,將其等之算術平均值作為平均纖維長度。 When the structure includes inorganic fibers, the average fiber length of the inorganic fibers is preferably 0.5 mm or more, and more preferably 1 mm or more, from the viewpoint of improving the formability and uniformity of the structure for cast production. Further, the average fiber length of the inorganic fibers is preferably 15 mm or less, more preferably 8 mm or less, and still more preferably 5 mm or less, from the viewpoint of improving the formability of the structure. Regarding the average fiber length of the inorganic fibers, first, the fibrous substances present as the inorganic fibers were determined and specified by the above-mentioned method for the fibrous substances existing on the surface of the structure. After that, 30 or more fibers were randomly selected from the two-dimensional screen when the inorganic fibers were observed under a microscope or SEM at a magnification of 50 times, and the lengths from one end to the other end were measured. The arithmetic mean thereof was taken as the average fiber length.
於結構體包含無機纖維之情形時,就提高鑄物製造用結構體之成形性及均勻性之觀點而言,無機纖維平均纖維直徑較佳為5 μm以上,更佳為10 μm以上。 又,關於無機纖維平均纖維直徑,就提高結構體之成形性,及提高製造時及澆鑄時之結構體之尺寸均勻性之觀點而言,較佳為30 μm以下,更佳為20 μm以下,進而較佳為15 μm以下。 關於無機纖維平均纖維直徑,以與上述無機纖維之判定方法相同之方式判定出存在無機纖維後,可以任意選出之30根以上之無機纖維為對象,對每根纖維測定5處與纖維之長度方向正交之長度,將其等之算術平均值作為平均纖維直徑。 When the structure contains inorganic fibers, the average fiber diameter of the inorganic fibers is preferably 5 μm or more, and more preferably 10 μm or more, from the viewpoint of improving the formability and uniformity of the structure for cast production. In addition, the average fiber diameter of the inorganic fibers is preferably 30 μm or less, more preferably 20 μm or less, from the viewpoints of improving the formability of the structure and improving the dimensional uniformity of the structure during production and casting. More preferably, it is 15 μm or less. Regarding the average fiber diameter of inorganic fibers, after judging the presence of inorganic fibers in the same manner as the above-mentioned method for judging inorganic fibers, 30 or more inorganic fibers can be arbitrarily selected as the object, and the length direction of the fibers at 5 locations for each fiber is measured. The arithmetic mean of the orthogonal lengths was taken as the average fiber diameter.
於不損害本發明之效果之範圍內,鑄物製造用結構體除上述成分以外可塗佈塗模劑。於該情形時,鑄物製造用結構體具備具有上述結構體之構成之基材部、及藉由塗模劑等之塗佈而於該基材部之表面形成之表面層。 塗模劑之目的在於改善金屬滲透防止性、表面平滑性及脫模性。 作為塗模劑,例如可例舉以耐火粒子為主原料且包含熱硬化性樹脂或矽酮等作為有機成分之材料等廣泛用於砂模鑄造或殼模鑄造等之材料。 再者,本發明之鑄物製造用結構體即便於未藉由塗佈塗模劑而形成表面層之情形時,金屬滲透防止性、表面平滑性及脫模性亦優異。 In the range which does not impair the effect of this invention, the mold coating agent can be applied to the structure for casting manufacture in addition to the above-mentioned components. In this case, the structure for casting production includes a base material portion having the structure described above, and a surface layer formed on the surface of the base material portion by application of a mold coating agent or the like. The purpose of the mold coating agent is to improve metal penetration resistance, surface smoothness and mold release properties. As a mold coating agent, the material widely used for sand mold casting, shell mold casting, etc., such as a material containing refractory particles as a main raw material and containing as an organic component such as a thermosetting resin, silicone, etc., is mentioned, for example. Furthermore, the structure for casting manufacture of this invention is excellent in metal penetration prevention property, surface smoothness, and mold release property even when the surface layer is not formed by applying a mold coating agent.
以下,對鑄物製造用結構體之製造方法進行說明。本製造方法大致分為下述步驟:將包含有機纖維之有機成分、及視需要而定之無機粒子或無機纖維等無機成分與分散介質混合,製作結構體前驅物;以及利用衝壓模具對上述結構體前驅物進行加熱按壓,將該結構體前驅物一面固化一面成形。 以下說明中,作為較佳之形態,例舉將包含有機纖維之有機成分與無機粒子混合,製作結構體前驅物之方法進行說明。 Hereinafter, the manufacturing method of the structure for casting manufacture is demonstrated. This production method is roughly divided into the following steps: mixing an organic component including organic fibers, and inorganic components such as inorganic particles or inorganic fibers as needed, and a dispersion medium to prepare a structure precursor; The precursor is heated and pressed, and the structure precursor is formed while curing. In the following description, as a preferable form, the method of mixing an organic component containing an organic fiber and an inorganic particle, and producing a structure precursor is demonstrated.
首先,將包含有機纖維之有機成分、無機粒子等無機成分、及分散介質混合,製作結構體前驅物(混合步驟)。 具體而言,將作為有機成分之有機纖維及熱硬化性樹脂、各種無機粒子、及分散介質均勻地混合,製作結構體前驅物。 結構體前驅物含有作為有機成分之有機纖維及熱硬化性樹脂、各種無機粒子、及分散介質,並且為麵團狀。 所謂麵團,係指具有流動性,能夠容易因外力而變形,並且混合之各種有機成分、各種無機成分及分散介質不易分離之狀態。 First, an organic component including organic fibers, inorganic components such as inorganic particles, and a dispersion medium are mixed to prepare a structure precursor (mixing step). Specifically, an organic fiber as an organic component, a thermosetting resin, various inorganic particles, and a dispersion medium are uniformly mixed to prepare a structure precursor. The structure precursor contains organic fibers and thermosetting resins as organic components, various inorganic particles, and a dispersion medium, and is in the form of a dough. The so-called dough refers to a state in which it has fluidity and can be easily deformed by external force, and the mixed organic components, various inorganic components and dispersion medium are not easily separated.
各種有機成分、各種無機粒子及分散介質之混合可藉由一次添加進行混合,亦可藉由按照任意順序依序添加進行混合。就混合之均勻性之觀點而言,較佳為將各種有機成分及各種無機粒子預先以乾式混合後,添加分散介質進行混合。 結構體前驅物例如可使用人工、或公知之混練裝置進行混練而製作。 於使用混練裝置之情形時,較佳為適合漿料或麵團等高黏度之攪拌之萬能攪拌機、捏合機或加壓式捏合機等。 於使用混練裝置之情形時,例如可使用加壓型捏合機(Nihon Spindle Manufacturing股份有限公司製造),以6.1 rpm混練30分鐘。 The mixing of various organic components, various inorganic particles, and dispersion medium may be performed by one addition or by sequential addition in any order. From the viewpoint of the uniformity of mixing, it is preferable to add and mix various organic components and various inorganic particles by dry mixing in advance. The structure precursor can be produced by kneading, for example, manually or using a known kneading apparatus. When a kneading device is used, it is preferably a universal mixer, a kneader, a pressurized kneader, etc., which are suitable for mixing high viscosity such as slurry or dough. In the case of using a kneading device, for example, a pressurized kneader (manufactured by Nihon Spindle Manufacturing Co., Ltd.) can be used, and kneading can be performed at 6.1 rpm for 30 minutes.
作為分散介質,可例舉水、乙醇、甲醇等溶劑或該等之混合系等水系分散介質。 就提高各種材料之分散穩定性及操作容易性之觀點而言,較佳為使用水作為分散介質。 相對於包含各種有機成分及各種無機粒子之固形物成分混合物之合計100質量份,水等分散介質之添加量較佳為10質量份以上70質量份以下。 The dispersion medium may, for example, be a solvent such as water, ethanol, or methanol, or an aqueous dispersion medium such as a mixed system of these. From the viewpoints of improving the dispersion stability and ease of handling of various materials, it is preferable to use water as a dispersion medium. The addition amount of a dispersion medium such as water is preferably 10 parts by mass or more and 70 parts by mass or less with respect to a total of 100 parts by mass of the solid content mixture containing various organic components and various inorganic particles.
於包含層狀黏土礦物作為無機粒子之情形時,層狀黏土礦物雖然於其乾燥狀態下為粒狀或粉狀,但藉由與水混合,與層狀黏土礦物之單位結晶層間所含之陽離子水合,水分子進入該層間。 關於濕潤狀態之層狀黏土礦物,層狀黏土礦物中單位結晶層間之距離因水分子而增加,而變得膨潤,成為具有黏性之流動體。 由於層狀黏土礦物之流動體兼具流動性與黏性,故可容易地進入與有機纖維或無機粒子等其他成分之間,並且可如將該等相互結合之黏合劑般發揮功能。 In the case of containing the layered clay mineral as inorganic particles, the layered clay mineral is granular or powdery in its dry state, but by mixing with water, the layered clay mineral is mixed with the cations contained in the unit crystal layer of the layered clay mineral. Hydration, water molecules enter the interlayer. Regarding the layered clay minerals in the wet state, the distance between the unit crystal layers in the layered clay minerals increases due to the increase of water molecules, and it becomes swelled and becomes a viscous fluid. Since the fluidity of layered clay minerals has both fluidity and viscosity, it can easily enter between other components such as organic fibers or inorganic particles, and can function as a binder that binds these to each other.
就提高製造結構體時之成形性及韌性,提高所得之結構體之操作性並且減少結構體之缺陷之觀點而言,結構體前驅物中有機纖維之含量相對於固形物成分總含量較佳為0.3質量%以上,進而較佳為0.5質量%以上。 就於使用所得之結構體進行澆鑄時,減少澆鑄時之氣體產生而減少鑄物之缺陷之觀點而言,有機纖維之含量較佳為10質量%以下,進而較佳為5質量%以下。 所用之有機纖維之平均纖維長度及平均纖維直徑可分別使用處於上述範圍內者。 From the viewpoints of improving the formability and toughness when manufacturing the structure, improving the handleability of the obtained structure, and reducing the defects of the structure, the content of the organic fibers in the structure precursor is preferably 10% relative to the total content of the solid content. 0.3 mass % or more, and more preferably 0.5 mass % or more. The content of organic fibers is preferably 10 mass % or less, and more preferably 5 mass % or less, from the viewpoint of reducing gas generation during casting and reducing defects of the casting when casting using the obtained structure. The average fiber length and the average fiber diameter of the organic fibers used can be used within the above ranges, respectively.
就使製造結構體時及澆鑄時之形狀保持性、表面平滑性及脫模性良好之觀點而言,結構體前驅物中相對於固形物成分含量之第1無機粒子含量較佳為40質量%以上,進而較佳為60質量%以上。 又,關於結構體前驅物中相對於固形物成分含量之無機粒子含量,就有效地表現出結構體之韌性,提高所得之結構體之操作性之觀點而言,較佳為90質量%以下,進而較佳為85質量%以下。 所用之第1無機粒子之平均粒徑可使用處於上述範圍內者。 The content of the first inorganic particles relative to the solid content in the structure precursor is preferably 40% by mass from the viewpoint of making the shape retention, surface smoothness, and releasability good at the time of production of the structure and at the time of casting above, more preferably 60 mass % or more. In addition, the inorganic particle content relative to the solid content in the structure precursor is preferably 90 mass % or less from the viewpoint of effectively expressing the toughness of the structure and improving the handleability of the obtained structure, More preferably, it is 85 mass % or less. The average particle diameter of the used first inorganic particles can be used within the above-mentioned range.
於結構體中包含第2無機粒子之情形時,就使鑄物製造用結構體之成形性良好之觀點而言,結構體前驅物中相對於固形物成分含量之第2無機粒子含量較佳為1質量%以上,更佳為3質量%以上,特佳為5質量%以上。 又,就於使用所得之結構體進行澆鑄時,抑制鑄造時來自結構體之氣體產生量,減少鑄物之氣體缺陷之產生率之觀點而言,結構體前驅物中相對於固形物成分含量之第2無機粒子含量較佳為50質量%以下,更佳為30質量%以下,進而較佳為20質量%以下。 於使用層狀黏土礦物作為第2無機粒子之情形時,可將層狀黏土礦物之含量設為上述範圍。 所用之第2無機粒子之平均粒徑可使用處於上述範圍內者。 When the structure contains the second inorganic particles, the content of the second inorganic particles relative to the solid content content in the structure precursor is preferably from the viewpoint of improving the formability of the structure for casting a casting. 1 mass % or more, more preferably 3 mass % or more, particularly preferably 5 mass % or more. In addition, from the viewpoint of suppressing the amount of gas generated from the structure during casting and reducing the rate of occurrence of gas defects in the casting when casting is performed using the obtained structure, the content of the solid content in the precursor of the structure is The second inorganic particle content is preferably 50 mass % or less, more preferably 30 mass % or less, and still more preferably 20 mass % or less. When the layered clay mineral is used as the second inorganic particles, the content of the layered clay mineral can be set to the above range. The average particle diameter of the used second inorganic particles can be used within the above-mentioned range.
結構體中可不含無機纖維,即結構體中無機纖維之含量可為0質量%,結構體中亦可含有無機纖維。於包含無機纖維之情形時,就提高製造結構體時之成形性及澆鑄時之形狀保持性之觀點而言,無機纖維之含量較佳為大於0質量%且為20質量%以下,更佳為16質量%以下,進而較佳為5質量%以下,進而更佳為3質量%以下。 於包含複數種無機纖維之情形時,無機纖維之含量以合計量為基準。 所用之無機纖維之平均纖維長度及平均纖維直徑可分別使用處於上述範圍內者。 The structure may not contain inorganic fibers, that is, the content of inorganic fibers in the structure may be 0% by mass, and the structure may also contain inorganic fibers. In the case of including inorganic fibers, the content of inorganic fibers is preferably more than 0 mass % and 20 mass % or less, and more preferably 16 mass % or less, more preferably 5 mass % or less, still more preferably 3 mass % or less. In the case of including a plurality of inorganic fibers, the content of the inorganic fibers is based on the total amount. The average fiber length and average fiber diameter of the inorganic fibers used can be used within the above ranges, respectively.
於包含碳纖維作為無機纖維之情形時,就提高製造結構體時之成形性及澆鑄時之形狀保持性之觀點而言,碳纖維之含量較佳為1質量%以上,更佳為2質量%以上。 又,碳纖維之含量較佳為20質量%以下,更佳為16質量%以下。 When carbon fibers are included as inorganic fibers, the content of carbon fibers is preferably 1 mass % or more, more preferably 2 mass % or more, from the viewpoint of improving the formability at the time of manufacturing the structure and the shape retention at the time of casting. Moreover, 20 mass % or less is preferable, and, as for content of carbon fiber, 16 mass % or less is more preferable.
就提高結構體之成形性之觀點而言,可將麵團狀之結構體前驅物供給至外力賦予機構進行延伸,製成片狀(延伸步驟)。 作為外力賦予機構,只要是能夠將結構體前驅物延伸為片狀之構成,則無特別限制,例如可將結構體前驅物供給至一對延伸輥之間、或延伸輥與平板之間進行延伸。 於該步驟之前後,結構體前驅物係維持為藉由外力而容易變形之狀態。 From the viewpoint of improving the formability of the structure, the dough-like structure precursor can be supplied to an external force imparting mechanism and stretched to form a sheet (stretching step). The external force applying means is not particularly limited as long as it can stretch the structure precursor into a sheet shape. For example, the structure precursor can be supplied between a pair of stretching rolls, or between stretching rolls and a flat plate, and stretched . Before and after this step, the structure precursor is maintained in a state easily deformed by an external force.
繼而,利用衝壓模具對麵團狀或片狀之結構體前驅物進行加熱按壓,將該結構體前驅物一面乾燥固化,一面成形為具有目標鑄模之形狀之結構體(成形步驟)。藉此,可獲得於結構體表面至少存在有機纖維之結構體。 衝壓模具具有與成形之鑄物製造用結構體之外形對應之形狀。藉由使用該衝壓模具對結構體前驅物進行加熱按壓,將衝壓模具之形狀轉印於結構體前驅物上,並且一面將結構體前驅物中所含之水分脫水,使其乾燥固化,一面成形為具有目標鑄模之形狀之結構體。與此同時,使可作為有機成分而包含之熱硬化性樹脂硬化。 經過該步驟之結構體變得不容易因外力而變形。成形之結構體可以具有朝向外部開口之模腔之方式成形,組合兩個一組之分割式模具成為鑄模,亦可成為一體成形之結構體。 Next, the dough-like or sheet-like structure precursor is heated and pressed with a stamping die, and the structure precursor is dried and solidified while being molded into a structure having the shape of the target mold (forming step). Thereby, a structure in which at least organic fibers are present on the surface of the structure can be obtained. The stamping die has a shape corresponding to the outer shape of the cast structure to be formed. By using the stamping die to heat and press the structure precursor, the shape of the stamping die is transferred to the structure precursor, and the moisture contained in the structure precursor is dehydrated, dried and solidified, and then shaped. It is a structure with the shape of the target mold. At the same time, the thermosetting resin which can be contained as an organic component is hardened. The structure after this step becomes less likely to be deformed by external force. The formed structure can be formed by having a cavity that opens to the outside, and a set of two split molds can be combined to form a casting mold, or it can be an integrally formed structure.
藉由加熱及按壓從結構體前驅物中將水分脫水,藉此該前驅物中所含之層狀黏土礦物失去於其單位結晶層間存在之水等分散介質分子。藉由失去分散介質分子,層狀黏土礦物一面與有機纖維及無機粒子等無機成分一起於結構體之內部形成緊密之結構一面收縮固化。 其結果,有機纖維、層狀黏土礦物及其他無機粒子之間產生剪力,變得不容易因外力而變形,同時可有效地發揮結構體之形狀保持性。 再者,關於有機纖維之纖維長及纖維直徑、各種無機粒子之粒徑及視需要含有之無機纖維之纖維長及纖維直徑,即便經過從結構體前驅物之製作至成形步驟之間所進行之混合、膨潤、乾燥及加熱按壓,該纖維長及纖維直徑以及粒徑亦幾乎沒有變化,故用作原材料之各種纖維之纖維長及纖維直徑以及各種粒子之粒徑與結構體中存在之各種纖維之纖維長及纖維直徑以及各種粒子之粒徑大致相同。 Water is dehydrated from the precursor of the structure by heating and pressing, whereby the layered clay minerals contained in the precursor lose the dispersion medium molecules such as water existing between the unit crystal layers. By losing the dispersing medium molecules, the layered clay minerals form a compact structure inside the structure together with inorganic components such as organic fibers and inorganic particles, while shrinking and solidifying. As a result, shear force is generated between organic fibers, layered clay minerals, and other inorganic particles, and it becomes difficult to deform by external force, and the shape retention of the structure can be effectively exhibited. Furthermore, with regard to the fiber length and fiber diameter of organic fibers, the particle diameters of various inorganic particles, and the fiber length and fiber diameter of inorganic fibers contained as needed, even after the process from the production of the structural precursor to the forming step. Mixing, swelling, drying, and heating and pressing, the fiber length, fiber diameter and particle size are also almost unchanged. Therefore, the fiber length and fiber diameter of various fibers used as raw materials, the particle size of various particles, and the various fibers existing in the structure are also almost unchanged. The fiber length, fiber diameter and particle size of various particles are roughly the same.
關於成形步驟中之加熱溫度,就容易地去除來自結構體前驅物之水等分散介質之觀點而言,較佳為70℃以上,更佳為100℃以上。 成形步驟中之加熱溫度較佳為250℃以下,更佳為200℃以下。 關於成形步驟中之加熱時間,就製造效率之觀點而言,以上述加熱溫度之範圍為條件,較佳為設為1分鐘以上60分鐘以下。 關於成形步驟中賦予之壓力,就提高結構體之成形性之觀點而言,較佳為0.5 MPa以上,更佳為1 MPa以上。 又,就提高結構體之成形性之觀點而言,較佳為20 MPa以下,更佳為10 MPa以下。 The heating temperature in the forming step is preferably 70° C. or higher, more preferably 100° C. or higher, from the viewpoint of easily removing a dispersion medium such as water from the structure precursor. The heating temperature in the forming step is preferably 250°C or lower, more preferably 200°C or lower. The heating time in the molding step is preferably 1 minute or more and 60 minutes or less under the condition of the above-mentioned heating temperature range from the viewpoint of production efficiency. The pressure applied in the forming step is preferably 0.5 MPa or more, more preferably 1 MPa or more, from the viewpoint of improving the formability of the structure. Moreover, from the viewpoint of improving the formability of the structure, it is preferably 20 MPa or less, more preferably 10 MPa or less.
關於鑄物製造用結構體,就減少由於源自水等分散介質之蒸氣所導致之鑄物之氣體缺陷之觀點而言,較佳為將其水分量設為5質量%以下,更佳為設為3質量%以下。 鑄物製造用結構體中之水分量可藉由上述成形步驟進行調節,亦可除加熱按壓步驟以外,進而藉由進行乾燥步驟來調節。 於進行乾燥步驟之情形時,可使用公知之恆溫槽或熱風乾燥裝置等。 又,乾燥步驟中之加熱溫度及加熱時間可與上述相同。 From the viewpoint of reducing the gas defect of the casting due to the vapor derived from a dispersion medium such as water, the structure for manufacturing a cast preferably has a water content of 5% by mass or less, and more preferably It is 3 mass % or less. The moisture content in the structure for casting manufacture may be adjusted by the above-mentioned forming step, or may be adjusted by performing a drying step in addition to the heating and pressing step. In the case of performing the drying step, a well-known constant temperature bath, a hot air drying device, or the like can be used. In addition, the heating temperature and heating time in the drying step may be the same as those described above.
於將包括兩個一組之分割式模具之鑄物製造用結構體組合成鑄模之情形時,依照上述方法以成為一組分割式模具之方式製作結構體後,以使模腔側成為內側之方式進而接合分割式模具,藉此可製造目標鑄模。 作為分割式模具之接合方法,例如可使用螺絲或夾具等接合構件、或通用接著劑、可覆蓋一組分割式模具之砂模等進行接合。 In the case of combining a casting mold including two sets of split molds into a casting mold, after the structure is fabricated to form a set of split molds according to the above method, the cavity side becomes the inner side. The method in turn joins the split mold, whereby the target mold can be produced. As a method of joining the divided molds, for example, a joining member such as a screw or a jig, a general-purpose adhesive, a sand mold that can cover a set of divided molds, or the like can be used for joining.
鑄物製造用結構體之厚度可據目標鑄物之形狀適當設定,但就獲得澆鑄時之充分之熱強度及形狀保持性之觀點而言,至少與熔融金屬相接之部分之厚度較佳為0.2 mm以上,更佳為0.5 mm以上,進而較佳為1 mm以上。 又,就提高結構體之操作容易性或減少氣體產生量之觀點而言,較佳為10 mm以下,更佳為5 mm以下。 結構體之厚度可藉由適當變更成形型之形狀或壓力而調整。 The thickness of the structure for casting casting can be appropriately set according to the shape of the target casting, but from the viewpoint of obtaining sufficient thermal strength and shape retention during casting, the thickness of at least the part in contact with the molten metal is preferably 0.2 mm or more, more preferably 0.5 mm or more, and still more preferably 1 mm or more. In addition, from the viewpoint of improving the ease of handling of the structure and reducing the amount of gas generated, it is preferably 10 mm or less, more preferably 5 mm or less. The thickness of the structure can be adjusted by appropriately changing the shape or pressure of the molding.
由於經過以上步驟而製造之鑄物製造用結構體包含有機纖維,故輕量且韌性較高,可抑制結構體之崩解或龜裂、破裂之產生,結構體之操作性亦優異。又,藉由於鑄物製造用結構體包含無機粒子,會成為輕量且表現出所需之韌性,同時耐熱性得到提高,兼具較高之常溫強度及熱強度、較高之形狀保持性之鑄物製造用結構體。 又,可有效地減少結構體對鑄物表面之金屬滲透、或氣體缺陷等鑄物缺陷。其結果,可製造尺寸精度或表面平滑性優異之鑄物。 可製造尺寸精度或表面平滑性優異之鑄物,意味著可減少用以使製造之鑄物達到所需之形狀或尺寸精度之後處理,其結果,可降低鑄物之製造成本。 Since the cast manufacturing structure produced by the above steps contains organic fibers, it is lightweight and has high toughness, and the disintegration of the structure, the occurrence of cracks and cracks can be suppressed, and the handleability of the structure is also excellent. In addition, since the structure for manufacturing a cast product contains inorganic particles, it becomes lightweight and exhibits the required toughness, and at the same time, the heat resistance is improved, and the structure has both high room temperature strength and hot strength, and high shape retention. Casting structure for manufacturing. Furthermore, casting defects such as metal penetration of the structure to the casting surface and gas defects can be effectively reduced. As a result, a cast product excellent in dimensional accuracy and surface smoothness can be produced. It is possible to manufacture a cast with excellent dimensional accuracy or surface smoothness, which means that the post-processing for making the manufactured cast to a desired shape or dimensional accuracy can be reduced, and as a result, the manufacturing cost of the cast can be reduced.
使用鑄物製造用結構體之鑄物之製造方法可藉由一般之鑄造方法進行。即,從鑄物製造用結構體中形成之澆注口注入熔融金屬,進行澆鑄。並且,完成澆鑄後,冷卻至特定溫度,除去鑄物製造用結構體,顯露出鑄物。其後,可視需要對鑄物實施修整處理等後處理。The manufacturing method of the casting using the structure for casting manufacture can be performed by a general casting method. That is, molten metal is poured from the sprue formed in the structure for casting product manufacture, and casting is performed. And after completion|finish of casting, it cools to a specific temperature, the structure for casting manufacture is removed, and a casting is exposed. After that, post-processing such as trimming treatment may be performed on the casting as necessary.
以上,對本發明基於其較佳之實施方式進行了說明,但本發明不受上述實施方式所限制,可適當組合各構成。 [實施例] As mentioned above, although this invention was demonstrated based on the preferable embodiment, this invention is not limited to the said embodiment, It is possible to combine each structure suitably. [Example]
以下,藉由實施例來更詳細地說明本發明。然而本發明之範圍並不受該實施例所限制。Hereinafter, the present invention will be described in more detail by way of examples. However, the scope of the present invention is not limited by this embodiment.
[實施例1] 使用有機纖維(機械紙漿)及熱硬化性樹脂(酚樹脂;可溶酚醛樹脂)作為有機成分,使用莫來石(球狀,平均粒徑為30 μm)作為第1無機粒子,且使用層狀黏土礦物粒子(蒙脫石;國峰工業股份有限公司製造,Kunipia F,平均粒徑為145 μm)作為第2無機粒子。 除此以外,使用PAN系碳纖維(Mitsubishi Chemical股份有限公司製造,PYROFILTR03CM A4G)作為無機纖維。 將該等按照以下表1中所示之比率混合各材料,製作結構體前驅物,依照上述方法製造鑄物製造用結構體。所得之鑄物製造用結構體製成如下兩種形狀:厚度2 mm之平板狀;及外徑為50 mm、長度為300 mm、厚度為2 mm之圓筒狀。再者,使用平板狀之鑄物製造用結構體,進行對後述之最大彎曲應力及最大彎曲應力時之彎曲應變、質量減少率、結構體表面之平均纖維長度、平均纖維直徑之各評價。又,使用圓筒狀之鑄物製造用結構體,進行對後述之結構體之操作性、澆鑄、澆鑄後之鑄物表面之表面性之各評價。 將水之添加量設為相對於混合物100質量份為50質量份。將結構體前驅物之加熱溫度及加熱時間設為140℃、10分鐘,成形步驟中之壓力設為5 MPa。 表中之「有機成分合計」表示鑄物製造用結構體中之有機成分之含量。本實施例中,未對結構體進行塗佈等處理,無表面層。 [Example 1] Organic fibers (mechanical pulp) and thermosetting resins (phenol resin; resol resin) were used as organic components, mullite (spherical, average particle size: 30 μm) was used as the first inorganic particles, and layered Clay mineral particles (montmorillonite; manufactured by Guofeng Industrial Co., Ltd., Kunipia F, average particle diameter: 145 μm) were used as the second inorganic particles. In addition to this, PAN-based carbon fibers (manufactured by Mitsubishi Chemical Co., Ltd., PYROFILTR03CM A4G) were used as inorganic fibers. These materials were mixed in the ratios shown in Table 1 below to prepare a structure precursor, and a structure for casting production was produced according to the above-mentioned method. The obtained structure for casting was formed into two shapes: a flat plate with a thickness of 2 mm; and a cylindrical shape with an outer diameter of 50 mm, a length of 300 mm, and a thickness of 2 mm. Furthermore, each evaluation of the maximum bending stress and the bending strain at the time of the maximum bending stress, the mass reduction rate, the average fiber length and the average fiber diameter on the surface of the structure, which will be described later, were performed using the flat-shaped casting structure. Moreover, each evaluation of the handleability of the structure described later, casting, and the surface property of the surface of the casting after casting was performed using the cylindrical casting structure. The addition amount of water was made into 50 mass parts with respect to 100 mass parts of mixtures. The heating temperature and heating time of the structure precursor were set at 140° C. for 10 minutes, and the pressure in the forming step was set at 5 MPa. "Total organic components" in the table indicates the content of the organic components in the structure for casting production. In this example, the structure was not subjected to treatment such as coating, and there was no surface layer.
[實施例2] 使用包含芳香族聚醯胺樹脂之纖維(東麗股份有限公司製造,Kevlar(註冊商標)短切纖維,芳香族聚醯胺樹脂100質量%)代替機械紙漿作為有機纖維,未使用無機纖維,除此以外,按照以下表1中所示之比率混合各材料,以與實施例1相同之方式製造鑄物製造用結構體。 [Example 2] Fibers containing aramid resin (manufactured by Toray Co., Ltd., Kevlar (registered trademark) chopped fibers, 100% by mass of aramid resin) were used as organic fibers instead of mechanical pulp, and inorganic fibers were not used, except In addition, each material was mixed in the ratio shown in the following Table 1, and the structure for casting manufacture was manufactured in the same manner as Example 1.
[實施例3] 除使用進行水中打漿處理提取紙漿纖維之報紙廢紙紙漿代替機械紙漿作為有機纖維以外,按照以下表1中所示之比率混合各材料,以與實施例1相同之方式製造鑄物製造用結構體。 [Example 3] A structure for casting production was produced in the same manner as in Example 1, except that newspaper waste paper pulp from which pulp fibers were extracted by water beating treatment was used instead of mechanical pulp as organic fibers, and the respective materials were mixed in the ratios shown in Table 1 below. .
[實施例4] 使用作為有機纖維之機械紙漿及熱硬化性樹脂(酚樹脂;可溶酚醛樹脂)作為有機成分,使用平均粒徑為27 μm之黑曜石(KINSEI MATEC股份有限公司製造,多面體狀,Nice Catch Flower#330)作為第1無機粒子。黑曜石中含有氧化鋁、二氧化矽及氧化鐵。 除此之外,使用PAN系碳纖維(Mitsubishi Chemical股份有限公司製造,PYROFIL TR03CM A4G)作為無機纖維。 除此以外,按照以下表1中所示之比率混合各材料,以與實施例1相同之方式製造鑄物製造用結構體。 [Example 4] Mechanical pulp as organic fibers and thermosetting resin (phenol resin; resol resin) were used as organic components, and obsidian with an average particle size of 27 μm (manufactured by KINSEI MATEC Co., Ltd., polyhedral shape, Nice Catch Flower #330) was used ) as the first inorganic particles. Obsidian contains alumina, silica and iron oxide. In addition to this, PAN-based carbon fibers (manufactured by Mitsubishi Chemical Co., Ltd., PYROFIL TR03CM A4G) were used as inorganic fibers. Except for this, each material was mixed in the ratio shown in the following Table 1, and the structure for casting manufacture was manufactured in the same manner as in Example 1.
[實施例5] 使用包含聚酯樹脂之纖維(纖維直徑11 μm,纖維長度5 mm,聚酯樹脂100質量%)代替機械紙漿作為有機纖維,未使用無機纖維,除此以外,按照以下表1中所示之比率混合各材料,以與實施例1相同之方式製造鑄物製造用結構體。 [Example 5] Fibers containing polyester resin (fiber diameter 11 μm, fiber length 5 mm, polyester resin 100% by mass) were used as organic fibers instead of mechanical pulp, and inorganic fibers were not used, except that the ratios shown in Table 1 below were used Each material was mixed, and the structure for casting manufacture was manufactured in the same manner as in Example 1.
[實施例6] 除使用包含聚酯樹脂之纖維(纖維直徑11 μm,纖維長度5 mm,聚酯樹脂100質量%)代替機械紙漿作為有機纖維以外,按照以下表1中所示之比率混合各材料,以與實施例1相同之方式製造鑄物製造用結構體。 [Example 6] The materials were mixed in the ratios shown in Table 1 below to implement the In the same manner as in Example 1, a structure for producing a cast was produced.
[比較例1] 除未使用有機纖維作為有機成分以外,按照以下表1中所示之比率混合各材料,以與實施例1相同之方式製造鑄物製造用結構體。 [Comparative Example 1] The respective materials were mixed in the ratios shown in Table 1 below, except that organic fibers were not used as the organic component, and a structure for casting production was produced in the same manner as in Example 1.
[比較例2] 除僅使用報紙廢紙紙漿代替機械紙漿及報紙廢紙紙漿之組合作為有機成分以外,按照以下表1中所示之比率混合各材料,以與實施例1相同之方式製造鑄物製造用結構體。 [Comparative Example 2] A structure for casting production was produced in the same manner as in Example 1, except that only newspaper waste paper pulp was used instead of the combination of mechanical pulp and newspaper waste paper pulp as the organic component, and the respective materials were mixed in the ratios shown in Table 1 below. .
[最大彎曲應力及最大彎曲應力時之彎曲應變之評價] 對於實施例及比較例之鑄物製造用結構體,藉由上述方法取出板狀之測定樣品,依據JIS K7017之三點彎曲試驗法對該樣品測定最大彎曲應力(MPa)及最大彎曲應力時之彎曲應變(%)。最大彎曲應力及彎曲應變係鑄物製造用結構體之韌性之指標,最大彎曲應力及彎曲應變之值越高,則結構體之韌性越高,結構體之操作性越高。將結果示於表1。 [Evaluation of Maximum Bending Stress and Bending Strain at Maximum Bending Stress] For the structures for the production of castings of the Examples and Comparative Examples, a plate-shaped measurement sample was taken out by the above method, and the maximum bending stress (MPa) and the maximum bending stress of the sample were measured according to the three-point bending test method of JIS K7017. Bending strain (%). The maximum bending stress and bending strain are indicators of the toughness of the structure for casting manufacturing. The higher the maximum bending stress and bending strain, the higher the toughness of the structure and the higher the operability of the structure. The results are shown in Table 1.
[質量減少率之評價] 實施例及比較例之鑄物製造用結構體之質量減少率之評價係使用熱重量測定裝置(Seiko Instruments股份有限公司製造,STA7200RV TG/DTA),將各實施例及各比較例之鑄物製造用結構體於氮氣氛圍下以升溫速度20℃/分鐘從30℃加熱至1000℃,測定其質量之變化作為溫度之函數,算出以30℃之時刻之質量為基準之質量減少率(%)。將結果示於表1。 [Evaluation of mass reduction rate] The evaluation of the mass reduction rate of the structures for the production of castings of Examples and Comparative Examples was performed by using a thermogravimetric measuring apparatus (manufactured by Seiko Instruments Co., Ltd., STA7200RV TG/DTA). The structure was heated from 30°C to 1000°C at a heating rate of 20°C/min in a nitrogen atmosphere, the change in mass was measured as a function of temperature, and the mass reduction rate (%) based on the mass at 30°C was calculated. The results are shown in Table 1.
[結構體表面之平均纖維長度、平均纖維直徑之評價] 實施例及比較例之存在於鑄物製造用結構體表面之有機纖維之平均纖維長度、平均纖維直徑之評價藉由上述方法進行。將結果示於表1。 [Evaluation of the average fiber length and average fiber diameter on the surface of the structure] The evaluation of the average fiber length and the average fiber diameter of the organic fibers present on the surface of the structure for producing a cast in Examples and Comparative Examples was performed by the above-described method. The results are shown in Table 1.
[結構體表面之纖維根數之評價] 實施例及比較例之存在於鑄物製造用結構體表面之有機纖維之纖維根數之評價藉由上述方法進行。將結果示於表1。 [Evaluation of the number of fibers on the surface of the structure] The evaluation of the number of fibers of the organic fibers present on the surface of the structure for producing a cast in Examples and Comparative Examples was performed by the above-mentioned method. The results are shown in Table 1.
[結構體之操作性之評價] 實施例及比較例之鑄物製造用結構體之操作性之評價藉由以下方法進行。具體而言,使用刀刃厚度為1 mm、縱鋸刀刃之手持鋸,於距離結構體之端面50 mm之位置進行切割,從切割端面測定於進行切割時產生之皸裂或缺漏之影響範圍長度(mm)。影響範圍長度越短,意味著結構體之操作性越良好。將結果示於以下表1。 [Evaluation of the operability of the structure] The evaluation of the workability of the structure for cast production of the Example and the comparative example was performed by the following method. Specifically, a hand-held saw with a blade thickness of 1 mm and a vertical saw blade was used to cut at a position 50 mm away from the end face of the structure, and the length of the influence range (mm ). The shorter the sphere of influence length, the better the operability of the structure. The results are shown in Table 1 below.
[澆鑄之評價(逆吹高度)] 將實施例及各比較例之鑄物製造用結構體作為鑄模,於20秒內向該鑄模中流入包含鑄鐵之1350℃之熔融金屬25 kg,製造鑄物。此時,測定來自熔融金屬流入口端面之熔融金屬之逆吹高度(mm)。逆吹高度越低,表示越能抑制流入熔融金屬時從鑄物製造用結構體中產生之氣體,越能減少鑄物之氣體缺陷,並且意味著澆鑄作業之安全性越高。將結果示於以下表1。 [Evaluation of casting (back blowing height)] Castings were produced by pouring 25 kg of molten metal at 1350°C containing cast iron into the casting molds for 20 seconds using the structures for producing casts of the Examples and Comparative Examples as molds. At this time, the blowback height (mm) of the molten metal from the end face of the molten metal inflow port was measured. The lower the blowback height is, the more the gas generated from the structure for casting a casting can be suppressed when the molten metal flows in, the more the gas defects of the casting can be reduced, and the higher the safety of the casting operation is. The results are shown in Table 1 below.
[鑄物表面之表面性評價] 將實施例及各比較例之鑄物製造用結構體作為鑄模,向該鑄模中流入包含鑄鐵之1350℃之熔融金屬,製造鑄物。算出此時形成之金屬滲透部分之面積比率,對鑄物表面之表面性進行評價。 具體而言,於鑄物製造用結構體與所得之鑄物之接觸部分之鑄物表面上,將流入之熔融金屬破壞鑄物製造用結構體並固著之部分,或者夾帶源自鑄砂之附著物並固著之部分視為金屬滲透部分,以目視判定其存在之有無及範圍。 其次,關於藉由上述方法而判定之金屬滲透部分之範圍,根據各金屬滲透部分之形狀切割基重固定之片材,將切割之片材之質量之總和除以片材之基重,藉此算出金屬滲透部分之面積。 又,關於鑄物之表面積,使用基重固定之片材,以該片材互不重疊之方式被覆鑄物表面,將用於被覆之片材之質量除以片材之基重,藉此算出鑄物之表面積。 然後,以金屬滲透部分之面積相對於鑄物之表面積之百分率(%)算出金屬滲透部分之面積比率。 金屬滲透部分之面積比率越低,意味著結構體對鑄物表面之金屬滲透越少,鑄物之尺寸精度或表面平滑性越優異。將結果示於以下表1。 [Surface evaluation of casting surface] Castings were produced by using the structures for producing casts of Examples and Comparative Examples as a mold, and pouring molten metal containing cast iron at 1350°C into the mold. The area ratio of the metal penetration portion formed at this time was calculated, and the surface property of the cast surface was evaluated. Specifically, on the surface of the casting at the contact portion between the structure for casting a casting and the obtained casting, the molten metal that flows in destroys the part where the structure for manufacturing a casting is fixed and is fixed, or entrains a part derived from the casting sand. The attached and fixed part is regarded as the metal penetration part, and the existence and extent of its existence are visually judged. Next, regarding the range of the metal penetration portion determined by the above method, a sheet with a fixed basis weight is cut according to the shape of each metal penetration portion, and the sum of the mass of the cut sheets is divided by the basis weight of the sheet, thereby Calculate the area of the metal penetration portion. The surface area of the cast is calculated by using a sheet with a fixed basis weight, coating the surface of the cast so that the sheets do not overlap each other, and dividing the mass of the sheet for coating by the basis weight of the sheet. The surface area of the casting. Then, the area ratio of the metal permeation part was calculated as the percentage (%) of the area of the metal permeation part with respect to the surface area of the casting. The lower the area ratio of the metal penetration portion, the less the metal penetration of the structure into the surface of the casting, the more excellent the dimensional accuracy or the surface smoothness of the casting. The results are shown in Table 1 below.
[表1]
如表1所示,實施例之鑄物製造用結構體由於含有特定量之包含有機纖維之有機成分,故與比較例之鑄物製造用結構體相比,最大彎曲應力及彎曲應變為特定值以上,結構體之韌性提高,因此可知結構體之操作性提高。又,實施例之鑄物製造用結構體由於含有特定量之包含有機纖維之有機成分,故結構體之質量減少率為特定值以下,因此亦可知能夠有效地減少所得之鑄物之氣體缺陷。又,關於實施例之鑄物製造用結構體,金屬滲透部分之面積比率與比較例相比亦為同等以下,因此可知能有效地減少結構體對鑄物表面之金屬滲透,獲得尺寸精度及表面平滑性優異之鑄物。As shown in Table 1, since the structure for manufacturing a cast of the Example contains a specific amount of an organic component including organic fibers, the maximum bending stress and the bending strain are specific values as compared with the structure for manufacturing a casting of the comparative example. As described above, since the toughness of the structure is improved, it can be seen that the handleability of the structure is improved. Moreover, since the structure for manufacture of the cast of the Example contained a specific amount of organic components including organic fibers, the mass reduction rate of the structure was below a specific value, and it was also found that the gas defect of the obtained cast could be effectively reduced. In addition, the area ratio of the metal penetration portion of the structure for manufacturing the casting of the example is equal to or less than that of the comparative example, so it can be seen that the metal penetration of the structure to the surface of the casting can be effectively reduced, and the dimensional accuracy and the surface can be obtained. Casting with excellent smoothness.
因此,本發明之鑄物製造用結構體操作性優異,並且可減少所得之鑄物之氣體缺陷及鑄物表面產生之金屬滲透。 尤其是,實施例1、3及4之鑄物製造用結構體藉由將無機纖維與少量有機纖維調配在一起,而能夠抑制氣體產生量,並且提高彎曲應力。 又,實施例5之鑄物製造用結構體僅使用有機纖維便能充分地滿足彎曲特性,同時大幅度降低了該結構體之製造成本。 [產業上之可利用性] Therefore, the structure for casting production of the present invention is excellent in handleability, and can reduce gas defects in the obtained casting and metal penetration on the surface of the casting. In particular, in the structures for manufacturing casts of Examples 1, 3 and 4, the amount of gas generation can be suppressed and bending stress can be increased by blending inorganic fibers with a small amount of organic fibers. In addition, the structure for producing a cast of Example 5 can sufficiently satisfy the bending characteristics by using only the organic fibers, and at the same time, the production cost of the structure can be greatly reduced. [Industrial Availability]
根據本發明,可提供一種操作性優異,並且可減少鑄物之氣體缺陷及於鑄物表面產生之金屬滲透之鑄物製造用結構體。ADVANTAGE OF THE INVENTION According to this invention, it is excellent in workability, and can provide the structure for casting manufacture which can reduce the gas defect of a casting and the metal penetration which generate|occur|produces in the casting surface.
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